MEERA Table User Manual - 2020

Instructions for use
7200.01XX
MEERA mobile operating table
IFU 7200.01 EN 11 2020-03-03

Copyright notice
All rights reserved.
Any duplication, adaptation or translation without prior written consent is prohibited unless otherwise provided
for in the relevant copyright laws.
© Copyright MAQUET GmbH
Subject to technical modification!

Due to further development of the product, the figures used and technical specifications given in these Instruc-
tions for Use may slightly differ from the current state of the product.
V11 03 03-03-2020
7200.01XX
IFU 7200.01 EN 11
Contents
Contents
1 Introduction .............................................................................................................. 9
1.1 How to use these operating instructions............................................................................................... 9
1.1.1 Abbreviations ......................................................................................................................... 9
1.1.2 Symbols and formatting ......................................................................................................... 10
1.1.3 Definitions .............................................................................................................................. 11
1.1.3.1 Design of safety notes......................................................................................... 11
1.1.3.2 Structure of notes ................................................................................................ 11
1.1.3.3 Definition for 3-dimensional coordinate system................................................... 12
1.1.3.4 Definition of inclination and tilt............................................................................. 12
1.1.3.5 Definition of hazardous location, Zone AP-M ...................................................... 13
1.1.3.6 Definition of permitted overall load ...................................................................... 13
1.1.3.7 Definition of protrusion ........................................................................................ 13
1.1.3.8 Definition Positioning- / Transporting .................................................................. 13
1.1.3.9 Definition of usage-related restrictions ................................................................ 14
1.1.3.10 Definition of patient orientation............................................................................ 14
1.1.3.11 Definition of CENTRAL position .......................................................................... 15
1.1.3.12 Definition of applied part...................................................................................... 16
1.2 Symbols used ....................................................................................................................................... 17
1.3 Disposal ................................................................................................................................................ 20
1.3.1 Old products........................................................................................................................... 20
1.3.2 Packaging .............................................................................................................................. 20
1.3.3 Batteries and rechargeable batteries ..................................................................................... 20
1.3.4 Pads and covers .................................................................................................................... 20
1.3.5 Used electrical devices .......................................................................................................... 20
1.4 Overview............................................................................................................................................... 21
1.4.1 Meera OR table with optional accessories............................................................................. 21
1.4.2 Hand controls......................................................................................................................... 22
1.5 Basic requirements ............................................................................................................................... 23
1.5.1 Use in accordance with the intended purpose ....................................................................... 23
1.5.2 Applicable standards.............................................................................................................. 23
1.5.3 MEERA OR table (7200.01XX).............................................................................................. 23
1.5.3.1 Intended purpose MEERA operating table (7200.01XX)..................................... 23
1.5.3.2 Variants ............................................................................................................... 24
1.5.4 Control devices, optional........................................................................................................ 24
1.5.5 Product features..................................................................................................................... 24
1.5.5.1 Essential performance......................................................................................... 24
1.5.5.2 Latex-free materials............................................................................................. 24
1.5.6 Reportable event.................................................................................................................... 24
2 Safety notes.............................................................................................................. 25
2.1 General safety notes ............................................................................................................................ 25
2.2 Safety notes for the OR table ............................................................................................................... 27
2.3 Safety notes regarding the use of accessories..................................................................................... 29
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2.4 Safety notes regarding service ............................................................................................................. 30

2.5 Safety notes regarding padding............................................................................................................ 31
2.6 Safety notes EMC................................................................................................................................. 32
3 Initial operation ........................................................................................................ 33

3.1 Storage ................................................................................................................................................. 33
3.2 Ambient conditions ............................................................................................................................... 33
3.3 Power supply ........................................................................................................................................ 33
3.4 Connecting the service interface .......................................................................................................... 34
3.5 IR code ................................................................................................................................................. 36
3.5.1 Grouping of IR codes according to product groups ............................................................... 36
3.5.2 Determining / specifying the IR code .................................................................................... 37
3.5.3 Carrying out a functional test ................................................................................................. 37
3.6 Venting the hydraulic oil ....................................................................................................................... 37
4 Hand controls and functions .................................................................................. 38

4.1 Overview of control devices.................................................................................................................. 38
4.2 Mounting the control device to the side rail .......................................................................................... 39
4.3 Override control panel .......................................................................................................................... 39
4.3.1 Control buttons and functions ................................................................................................ 40
4.4 Corded hand controls ........................................................................................................................... 41
4.4.1 Connecting/removing corded control devices ........................................................................ 41
4.4.2 Foot switch (1009.81J0/J1/J2) ............................................................................................... 42
4.5 Universal control device (1009.25A0)................................................................................................... 43
4.5.1 Notes on use.......................................................................................................................... 43
4.5.2 Acoustic signals of the control device .................................................................................... 44
4.5.3 Button assignment and functions........................................................................................... 44
4.6 Adjustment functions ............................................................................................................................ 45
4.6.1 Adjusting the height of the OR table ...................................................................................... 45
4.6.2 Adjusting the back plate......................................................................................................... 45
4.6.3 Adjusting the leg plates.......................................................................................................... 46
4.6.4 Balancing the leg plate........................................................................................................... 47
4.6.5 Inclining the table top ............................................................................................................. 48
4.6.6 Tilting the table top laterally ................................................................................................... 49
4.6.7 Moving the table top longitudinally......................................................................................... 50
4.6.8 Moving the table top to the horizontal position....................................................................... 51
4.6.9 Deactivating the lock function temporarily ............................................................................. 52
4.7 Operating menu .................................................................................................................................... 52
4.7.1 Display start screen ............................................................................................................... 52
4.7.2 Symbols for status bar ........................................................................................................... 53
4.7.3 Main menu [Menu] ................................................................................................................. 54
4.7.4 Connect the OR table ............................................................................................................ 54
4.7.4.1 Connecting a new OR table ................................................................................ 55
4.7.4.2 Reconnecting the known OR table...................................................................... 56
4.7.4.3 OR table is renamed ........................................................................................... 56
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4.7.4.4 Disconnect the OR table ..................................................................................... 57

4.7.4.5 Show IR code ...................................................................................................... 57
4.7.5 Menu [Device Settings] .......................................................................................................... 58
4.7.5.1 Set the brightness on the touchscreen................................................................ 58
4.7.5.2 Set the language ................................................................................................. 58
4.7.5.3 Resetting the control device ................................................................................ 59
4.7.5.4 Calling up system information ............................................................................. 60
4.7.6 Set the patient orientation ...................................................................................................... 61
4.7.7 Select the preset patient position........................................................................................... 63
4.7.8 User-defined patient positions ............................................................................................... 64
4.7.8.1 Save user-defined patient positions .................................................................... 64
4.7.8.2 Selecting a user-defined patient position ............................................................ 65
4.7.8.3 Editing user-defined patient positions ................................................................. 66
4.7.8.4 Quick saving user-defined patient positions........................................................ 67
4.7.8.5 Move to quick-save memory position .................................................................. 68
4.7.9 OR table adjustment function or lock / unlock button............................................................. 68
5 Operation and use.................................................................................................... 70

5.1 General ................................................................................................................................................. 70
5.2 OR table ............................................................................................................................................... 71
5.2.1 Acoustic signals issued by the OR table................................................................................ 71
5.2.2 Setting up equipotential bonding............................................................................................ 72
5.2.3 Status indicators mains connection / battery charge state..................................................... 72
5.2.3.1 Overview of status display for mains connection ................................................ 72
5.2.3.2 Overview of status display for battery charge state............................................. 73
5.2.4 Battery operation.................................................................................................................... 74
5.2.5 Deep discharge protection ..................................................................................................... 74
5.2.5.1 Automatic deep discharge................................................................................... 74
5.2.5.2 Activate deep discharge protection manually...................................................... 74
5.2.6 Charge batteries (mains operation) ....................................................................................... 75
5.2.7 Displacing / locking the OR table ........................................................................................... 76
5.2.7.1 Status display [LOCK] / [UNLOCK] ..................................................................... 77
5.2.7.2 Moving the OR table without autodrive [UNLOCK] ............................................. 77
5.2.7.3 Moving the OR table using autodrive [UNLOCK] ................................................ 78
5.2.7.4 Locking the OR table [LOCK] .............................................................................. 79
5.3 Table tops and accessories .................................................................................................................. 80
5.3.1 Mounting the table width extensions (1001.75A0 / 76A0)...................................................... 80
5.3.2 Mounting / removing the head rest ........................................................................................ 81
5.3.2.1 Mounting and removing the head rest using the head rest adapter (1130.81A0) 81
5.3.3 Extension plate (1131.31BC) ................................................................................................. 83
5.3.4 Mounting and removing the seat plate extension (1131.55BC ) ............................................ 84
5.3.5 Mounting / removing the leg plates ........................................................................................ 85
5.3.5.1 Mounting / removing the pair of leg plates (1133.53BC) ..................................... 85
5.3.5.2 Mounting / removing the leg plate (1133.58BC).................................................. 86
5.3.6 Attaching the X-ray top (1131.80A0), optional ....................................................................... 87
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5.3.6.1 Mounting / removing the X-ray top ...................................................................... 88

5.3.7 Removing / mounting pads .................................................................................................... 89
5.4 Explanation of instructions for use........................................................................................................ 90
5.4.1 CENTRAL position................................................................................................................. 90
5.4.2 Maximum height when moving the OR table with an overall load of up to 250 kg................. 90
6 Approved accessories and table top configuration ............................................. 91

6.1 Table top configuration for an overall load up to 155 kg....................................................................... 93
6.1.1 NORMAL patient orientation / OR table can be moved (UNLOCK)....................................... 93
6.1.2 REVERSE patient orientation/ OR table can be moved (UNLOCK) ...................................... 95
6.1.3 NORMAL patient orientation/OR table locked (LOCK) .......................................................... 97
6.1.4 REVERSE patient orientation/OR table locked (LOCK) ........................................................ 99
6.2 Table top configuration with an overall load of 155-250 kg .................................................................. 101
6.2.1 NORMAL patient orientation / OR table can be moved (UNLOCK)....................................... 101
6.2.2 REVERSE patient orientation / OR table can be moved (UNLOCK) ..................................... 103
6.2.4 REVERSE patient orientation/OR table locked (LOCK) ........................................................ 106
6.3 Table top configuration with an overall load of 250–450 kg ................................................................. 108
6.3.1 Usage-related restrictions for 250-454 kg.............................................................................. 108
6.4 Approved accessories .......................................................................................................................... 110
6.4.1 Side rail accessories .............................................................................................................. 110
6.4.2 Hand controls......................................................................................................................... 110
6.4.3 Maximum overall load up to 155 kg ....................................................................................... 110
6.4.3.1 Accessories for NORMAL mounting point up to 155 kg ...................................... 110
6.4.3.2 Accessories for the NORMAL mounting point up to 155 kg, OR table locked
(LOCK) ................................................................................................................ 111
6.4.3.3 Accessories for REVERSE mounting point up to 155 kg .................................... 112
6.4.3.4 Accessories for the REVERSE mounting point up to 155 kg, OR table locked
(LOCK) ................................................................................................................ 113
6.4.4 Maximum overall load 155–250 kg ........................................................................................ 113
6.4.4.1 Accessories for NORMAL interface from 155–250 kg......................................... 113
6.4.4.2 Accessories for REVERSE mounting point 155–250 kg ..................................... 114
6.4.4.3 Accessories for the REVERSE mounting point up to 250 kg, OR table locked
(LOCK) ................................................................................................................ 115
6.4.5 Maximum overall load 250–454 kg ........................................................................................ 115
6.4.5.1 Accessories for NORMAL interface from 250-454 kg ......................................... 115
6.4.5.2 Accessories for REVERSE mounting point 250–454 kg ..................................... 116
6.5 Projection.............................................................................................................................................. 116
6.5.1 Protrusion with a NORMAL patient orientation ...................................................................... 116
6.5.2 Protrusion with a REVERSE patient orientation .................................................................... 117
6.5.3 Maximum height with moveable OR table (UNLOCK) ........................................................... 117
7 Display notes............................................................................................................ 118

7.1 Structure of display notes ..................................................................................................................... 118
7.2 Notes on use ........................................................................................................................................ 118
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7.3 Warning notes / Status messages ........................................................................................................ 120
8 Cleaning and disinfection ....................................................................................... 122

8.1 General information .............................................................................................................................. 122
8.1.1 No mechanical preparation .................................................................................................... 123
8.1.2 Padding.................................................................................................................................. 124
8.2 Cleaning agents and disinfectants........................................................................................................ 125
8.2.1 Suitable cleaning agents........................................................................................................ 125
8.2.2 Suitable disinfectants ............................................................................................................. 125
8.2.3 Non-usable products / substances......................................................................................... 125
8.3 Prepare the OR table for cleaning ........................................................................................................ 126
8.4 Manual preparation............................................................................................................................... 126
8.4.1 Pre-cleaning........................................................................................................................... 126
8.4.2 Disinfection ............................................................................................................................ 126
8.4.3 Drying..................................................................................................................................... 126
8.4.4 Inspections............................................................................................................................. 126
9 Maintenance ............................................................................................................. 127

9.1 Visual and functional inspections ......................................................................................................... 127
9.2 Malfunctions and troubleshooting ......................................................................................................... 129
9.2.1 OR table................................................................................................................................. 129
9.2.2 IR remote control ................................................................................................................... 131
9.3 Inspection and Maintenance................................................................................................................. 132
9.4 Maintenance of corded hand controls .................................................................................................. 132
9.5 Repair ................................................................................................................................................... 132
9.6 Type plate position ............................................................................................................................... 133
9.7 Replacing fuse/setting the mains voltage ............................................................................................. 134
10 Technical specifications.......................................................................................... 135

10.1 General specifications .......................................................................................................................... 135
10.2 Ambient conditions ............................................................................................................................... 135
10.3 Surface temperature of application set ................................................................................................. 135
10.4 Noise level ............................................................................................................................................ 135
10.5 Electrical specifications ........................................................................................................................ 135
10.6 Weight .................................................................................................................................................. 136
10.7 Dimensions ........................................................................................................................................... 136
10.8 Adjustment ranges................................................................................................................................ 137
10.8.1 Longitudinal shift .................................................................................................................... 137
10.8.2 Inclination............................................................................................................................... 137
10.8.3 Tilt .......................................................................................................................................... 138
10.8.4 Back plate .............................................................................................................................. 138
10.8.5 Leg plate ................................................................................................................................ 139
10.9 Table top positions ............................................................................................................................... 140
10.9.1 FLEX position......................................................................................................................... 140
10.9.2 REFLEX position.................................................................................................................... 141
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10.9.3 BEACH CHAIR position ......................................................................................................... 142

10.10Electromagnetic compatibility (EMC).................................................................................................... 143
10.10.1 Cable lengths ......................................................................................................................... 143
10.10.2 Electromagnetic emissions .................................................................................................... 143
10.10.3 Resistance to electromagnetic interference........................................................................... 143
Index.......................................................................................................................... 146
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Introduction
How to use these operating instructions 1
1 Introduction
1.1 How to use these operating instructions

These operating instructions are provided to familiarise you with the features of this product. The
operating instructions are divided into separate chapters.
Please note:
• Read these operating instructions through carefully and completely before using the product
for the first time.
• Always proceed in accordance with the information provided in these operating instructions.
• Store these operating instructions in the vicinity of the product.
1.1.1 Abbreviations
EC European Community
EMC Electromagnetic compatibility
EN European standard
EEC European Economic Community
HD Harmonization document
HF High Frequency
IEC International Electrotechnical Commission
INT Intermittent
IP International Protection (type of protection against ingress of solid bodies
and liquids)
IPS Internal Power Source
IR Infrared
ISO International Organization for Standardization
LED Light-Emitting Diode
MDD Medical Devices Act
OR table Operating table
PUR Polyurethane integral foam
RF Radio frequency
SELV Safety Extra Low Voltage
SFC Soft Foam Core (special foam core)
SN Serial no.
UL Underwriters Laboratories Inc.
UPS Uninterrupted Power Supply
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Introduction
1 How to use these operating instructions
1.1.2 Symbols and formatting
Symbol Meaning
1. Instructions to follow / list with numbered steps
2.
Result of an action
● Numbered steps / List entry / precondition
Reference to other pages within this document
[...] Key / Module / Mode
bold Menu / on-screen button
[italics] Field to be filled in
1122.33XX Order number with different variants (XX)
Tab. 1: Symbols and formatting
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Introduction
1.1.3 Definitions
1.1.3.1 Design of safety notes
Pictogram Descriptor Text

DANGER! Identifies an immediate danger to people, which may
result in death or serious injuries.
WARNING! Identifies a potential danger to people or property, which

may result in damage to health or serious property dam-
ages.
CAUTION! Identifies a potential danger to property, which may res-

ult in property damages.
Tab. 2: Design of safety notes
1.1.3.2 Structure of notes
Pictogram Descriptor Explanation

NOTE Supplementary assistance or further useful information
which does not indicate a risk of injury to persons or a
risk of property damage are described in the text of the
note.
ENVIRONMENT Information regarding proper disposal.
Tab. 3: Structure of notes
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Introduction
1.1.3.3 Definition for 3-dimensional coordinate system
Reference X axis Y axis Z axis

Product Longitudinal direction Lateral direction Height
Patient Longitudinal Transverse Sagittal
Neutral Horizontal Horizontal Vertical
Fig. 1: Definition of terms for the 3-dimensional coordinate system
1 Frontal plane (horizontal plane) 3 Transverse plane

2 Sagittal plane
1.1.3.4 Definition of inclination and tilt
Fig. 2: Definition of inclination and tilt
1 Reverse Trendelenburg 3 Lateral tilt

2 Trendelenburg (head down) 4 Inclination
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Introduction
1.1.3.5 Definition of hazardous location, Zone AP-M

The term "AP-M zone" 1 is used to refer to the medical environment.
Fig. 3: Area with a risk of explosions, AP-M zone
1.1.3.6 Definition of permitted overall load

The maximum permitted overall load is derived by adding the patient weight, side rail accessory
weights and weight of positioning aids. The maximum permitted overall load is the maximum load
that may be placed on the table top.
Restrictions may result from special patient positioning devices or the accessories used for which
other weight loads may apply.
1.1.3.7 Definition of protrusion

Protrusion is the gap between the mounting point(s) of a table top to the relevant outer edge of
the table top components (e.g. head rest, leg plates) applied to the front.
The maximum protrusion of a table top may not be exceeded.
1.1.3.8 Definition Positioning- / Transporting

When moving, a distinction is made between moving the mobile operating table with a patient
and without a patient.
Positioning
Positioning refers to the process of moving the mobile operating table with a patient and within
the operating room.
Transporting
Transporting refers to the process of moving the mobile operating table without a patient in the
operating room.
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Introduction
1.1.3.9 Definition of usage-related restrictions

As of certain overall load thresholds and when moving the mobile operating table, one or more of
the following usage-related restrictions apply:
• Use of accessories
• Protrusion
• Adjustment functions
• Patient orientation
• Moving the operating table
The specific usage-related restrictions are listed in the chapter on tabletop configurations
[8 Page 91] in the appropriate sub-chapters.
1.1.3.10 Definition of patient orientation
WARN IN G !
Risk of injury!
Incorrectly adjusted patient orientation may cause adjustment of the OR
table in a direction that was not intended.
Check the correct patient orientation prior to making any adjustments.
The patient orientation is indicated in the status bar on the display on the hand
control.
The patient orientation is based on the position of the patient on the table compared to the OR
table base.
NORMAL patient orientation
The upper part of the patient's body is located

above the longer section of the OR table base
1.
Fig. 4: NORMAL patient orientation
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Introduction
REVERSE patient orientation
The legs are located above the longer section

of the OR table base 1 .
Fig. 5: REVERSE patient orientation
1.1.3.11 Definition of CENTRAL position
Fig. 6: CENTRAL position
With an overall load of 250 kg, the OR table may only be used if the OR table is in the CENTRAL
position: The longitudinal shift of the OR table is lifted and the centre table top bar 1 is above
the column 2 .
The table top stops at the CENTRAL position during a longitudinal shift. depending on the OR
table used, the longitudinal shift is then automatically continued or must be continued by pressing
the button once again.
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Introduction
1.1.3.12 Definition of applied part
Fig. 7: Applied part, OR table: Table top
The applied part of the OR table is the table top.
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Introduction
Symbols used 1
1.2 Symbols used

Symbols are attached to products, type plates and packaging.
Symbols Labelling
Labelling of products developed and marketed in accordance with relevant
European legal provisions.
UL classification mark from Underwriters Laboratories as proof that the

product has been assessed by Underwriters Laboratories for specific proper-
ties in order to exclude risks and to confirm the usability under certain circum-
stances.
This labelling signifies compliance with the requirements both for the USA and
for Canada.
Labelling in accordance with the standard ISO 15223-1.
Symbol for "Catalogue number / product number".
Labelling in accordance with the ISO 15223-1 standard.

Symbol for "Serial number".
Symbol for the labelling of medical devices
Labelling in accordance with the standard ISO 15223-1.

Symbol for "Name and address of the manufacturer". The date of manufactur-
ing can be combined with this symbol.

Symbol for "Consult instructions for use".
Marking according to the standard ISO 15223-1.

Symbol for "Pay attention to the supplied documents".
Labelling in accordance with the IEC 60601-1 standard.

Symbol for "Follow Instructions for use".
Tab. 4: Symbols
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Introduction
1 Symbols used
Symbols Labelling
Labelling of devices with an applied part of Type B in accordance with the IEC
60601-1 standard.
Level of protection against electric shock.
Labelling in accordance with the IEC 60601-1 standard.

Symbol for "Class II Equipment"
Labelling in accordance with the 2012/19/EU directive (on used electrical

equipment and electronics).
Symbol for "Do not dispose of product via the municipal collection points for
used electrical equipment".
Labelling in compliance with the IEC 60529 standard.

Symbol for "Splash protection".
Labelling in compliance with the IEC 60601-1 standard.

Symbol for "Equipotentiality".
Labelling of devices in the AP class in accordance with the IEC 60601-1

standard.
Explosion protection ensured by the avoidance of ignition sources when using
flammable blends of anaesthetics that are mixed with air, oxygen or nitrous
oxide.
Marking in compliance with the standard ISO 7010
Symbol for “warning concerning injury to hands e.g. Hazard of crushing,
shearing

Labelling of packaging materials.
Symbol for "Keep dry".

Symbol for "Fragile! Handle with care".
Labelling in accordance with the ISO 7000 standard.

Symbol for "Top".

Symbol for "Temperature limit".
Tab. 4: Symbols
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Introduction
Symbols used 1
Symbols Labelling
Symbol for "Humidity limitation".

Symbol for "Atmospheric pressure limitation".
Tab. 4: Symbols
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Introduction
1 Disposal
1.3 Disposal
1.3.1 Old products

Getinge will take back used products or those which are no longer in service. For further informa-
tion, please contact your personal Getinge representative.
Used products or parts thereof may be contaminated. In order to prevent a potential infection, the
product must be cleaned and disinfected prior to its return/disposal.
The national regulations and disposal regulations must be observed for all disposal measures.
1.3.2 Packaging
The packing materials are made of materials compatible with the environment. The packing ma-
terial may be disposed of by Getinge on request.
1.3.3 Batteries and rechargeable batteries

Rechargeable batteries/batteries can be submitted to your regional disposal system.
ENVI RO NMEN T
Defective rechargeable batteries must be recycled in accordance with guideline
2006/66/EC.
Defective rechargeable batteries may not be opened, disposed of in household
waste, burned or thrown in water.
Defective rechargeable batteries should be returned to local collection points.
1.3.4 Pads and covers

Pads and covers may be disposed of via the household waste.
1.3.5 Used electrical devices
Within the European Economic Community

This product is within the scope of the validity of guideline 2012/19/EU (waste electrical and elec-
tronic equipment). This product is not registered for use in private households, it may also not be
disposed of disposal via municipal collection points for waste electrical and electronic equipment.
For further information on legally compliant disposal, please contact the assigned Getinge repres-
entative.
Outside the European Economic Community

When disposing of this product, ensure compliance with the applicable national regulations on
the handling and disposal of used electrical equipment.
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Introduction
Overview 1
1.4 Overview
1.4.1 Meera OR table with optional accessories
5 6
1 2 3 4
9 8
10
12
11
13
14
Fig. 8: Overview of OR table (7200.01XX)
1 Head rest (1130.64A0/C0/D0/F0/G0), op- 8 REVERSE mounting point (leg plate mount-
tional ing point)
2 Head rest mounting point 9 Side rail
3 Extension plate (1131.31BC/FC), optional 10 Infrared receiver
4 NORMAL mounting point (back plate mount- 11 Socket for corded control device (corded
ing point) control device, foot switch)
5 Back plate 12 Override control panel
6 Seat plate 13 OR table base
7 Leg plate (1133.53BC/FC), optional 14 Mains connection
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Introduction
1 Overview
1.4.2 Hand controls
1 2
3
7
5
Fig. 9: Overview of control devices
1 IR remote control (7200.91A0), optional 6 Stationary charging station (1009.71A0) for

2 Corded control device (7200.90A0), optional IR remote control (7200.91A0), optional
3 Foot switch (1009.81J0/J1/J2), optional 7 Stationary charging station (1009.24A0/C0)
for universal control device (1009.25A0), op-
4 Universal control device (1009.25A0) tional
5 Mobile charging unit (1009.70A0) for IR re- 8 Mobile charging station (1009.24B0) for uni-
mote control (7200.91A0), optional versal control device (1009.25A0), optional
9 SENSOR DRIVE (1009.69XX)
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Introduction
Basic requirements 1
1.5 Basic requirements
1.5.1 Use in accordance with the intended purpose

This product is a medical device.
The product may only be operated by persons who have been instructed in the use of the product
by an authorised person.
The product is designed solely for the purpose of human medicine.
The patient may only be placed and positioned under medical supervision.
Rooms used for medical purposes in which the product is operated must comply with HD
60364-7-710 or equivalent national regulations.
The EMC characteristics of this product allow its use in industrial and hospital environments
(CISPR 11, Class A). This product may not provide adequate protection against radio services
when used in a residential environment (which typically requires Class B according to CISPR 11).
If necessary, the user must take corrective measures such as conversion or reorientation of the
product.
Accessories
Accessories or combinations of accessories may only be used as and when indicated in these in-
structions for use.
Other accessories, combinations of accessories or consumables may only be used if they are de-
signed specifically for the use in question and will not adversely affect either performance fea-
tures or safety requirements.
1.5.2 Applicable standards

The product meets the basic safety and performance requirements in accordance with the local
applicable legal specifications for medical devices.
1.5.3 MEERA OR table (7200.01XX)
1.5.3.1 Intended purpose MEERA operating table (7200.01XX)

The OR table is designed for the placement and positioning of the patient for surgical treatment
immediately before, during and after surgical interventions, as well as for examination and treat-
ment.
The table top is radiolucent and enables the intraoperative use of x-ray equipment. The design of
the table top means that it is suitable for all surgical disciplines. The product may only be oper-
ated by medically trained staff within the OR environment. Any use other than that described
above is deemed not to be in accordance with the intended purpose.
For patient positions and adjustment functions, such as longitudinal shift, tilt and inclination, the
OR table can be used for a maximum total load of 250 kg without restrictions. In the event of an
overall load on the table top of between 250 kg and 454 kg, the OR table may with used with re-
strictions. The OR table may be used for the transportation of patients within the OR sector only
and with restrictions in place.
The OR table may not be used under the following conditions:
• With a maximum overall load exceeding 454 kg
• With a maximum overall load exceeding 250 kg without taking the restrictions into account
• With accessories that are not approved by MAQUET
• In rooms with Magnetic Resonance Tomography equipment that is not approved by Maquet
7200.01XX
IFU 7200.01 EN 11 23 / 150
Introduction
1 Basic requirements
1.5.3.2 Variants
The product is available in the following versions:
• 7200.01B0
with SFC pad, without autodrive, EU side rail variant
• 7200.01B2
with SFC pad, with autodrive, EU side rail variant
• 7200.01F0
with SFC pad, without autodrive, US side rail variant
• 7200.01F2
with SFC pad, with autodrive, US side rail variant
1.5.4 Control devices, optional

The MEERA OR table can be power-adjusted using the following control devices:
• Universal control device (1009.25A0)
• Corded control device (7200.90A0)
• IR remote control (7200.91A0)
• Foot switch (1009.81J0/J1/J2)
• Override control panel on the column (integrated into the column)
1.5.5 Product features
1.5.5.1 Essential performance

The product corresponds to IEC 60601-1 and its collateral standards with the following essential
performance features:
• Ensure positioning quality and comfort using sufficient table top surface and appropriate posi-
tioning geometry
• Placement of the patient (or the patient’s body parts) without unwanted movement in case of
an initial error.
Note: For the use of HF surgery devices in conjunction with the product, the requirements must
be met in accordance with IEC 60601-1-2 and IEC 60601-2-46.
During the use of HF surgery devices in the vicinity of the product, due to electro magnetic radi-
ation, the essential electrical performance characteristics (adjustment functions) of the system
may not be executed or may only be executed at intervals.
1.5.5.2 Latex-free materials

All used materials (e.g. materials for pads and straps) are latex free.
1.5.6 Reportable event

Any serious incident involving this product must be reported to MAQUET GmbH and, if neces-
sary, to the local competent authority.
7200.01XX
24 / 150 IFU 7200.01 EN 11
Safety notes
General safety notes 2
2 Safety notes
2.1 General safety notes
DA NG ER !
Potentially fatal!
Risk caused by unauthorised modifications.
Modifications at the product are not permitted.
DA NG ER !
Potentially fatal!
Risk posed to the patient's vital functions due to incorrect positioning.
Position the patient correctly and keep under permanent observation.
WARN ING !
Risk of injury!
Improper patient positioning may cause health damage (e. g. decubitus).
Position the patient correctly and keep under constant observation.
WARN ING !
Risk of injury!
Faulty or defective products may result in injuries.
• Before use, check the proper working order and fully functional state of the
product.
• Stop using faulty or defective products and inform the Getinge representative.
WARN ING !
Risk of injury!
Getinge products may be used only when lubricated.
Lubricate Getinge products at regular intervals.
WARN ING !
Risk of burns!
The use of high-frequency devices, defibrillators and defibrillator monitors
exposes the patient to burn risks due to contact with the metal components
in the product or accessories and/or as a result of resting on wet drapes or
electrically conductive padding.
Avoid any contact between the patient and metal components; never use damp or
wet surgical drapes.
Be absolutely sure to comply with the manufacturers instructions for use!
WARN ING !
Risk of injury!
Magnetic fields with a magnitude greater than 0.5 mT may influence the func-
tionality of the product.
Never use the product within the 0.5 mT field.
WARN ING !
Risk of injury!
Functional restrictions to the product may be caused as a result of service
and maintenance work.
Do not carry out service and maintenance work to the product during an operation.
7200.01XX
IFU 7200.01 EN 11 25 / 150
Safety notes
2 General safety notes
WARN IN G !
Risk of injury!
If the patient is not secured, particularly when adjusting/moving, the patient
and/or their extremities may slip in an uncontrolled manner.
Always secure the patient using suitable aids (e.g. straps) and maintain continuous
observation.
WARN IN G !
Risk of injury!
When adjusting, moving or storing the OR table / table top, the staff, the pa-
tient and the accessories are exposed to pinching and shearing hazards, par-
ticularly in the area around the joints at the head rest, back and leg plates.
Always ensure that no one can be subjected to pinching or shearing action or in-
jured in any other way and that the accessories do not collide with any nearby ob-
jects.
WARN IN G !
Risk of injury!
When adjusting and moving the OR table, the table top or the accessories,
collisions may occur with the patient, between the individual products or
parts pointing downwards.
During the adjustment procedures, always pay attention to the OR table and ac-
cessories and avoid collisions. Ensure that tubes, cables and drapes are not
trapped.
WARN IN G !
Risk of injury!
If locking elements (eccentric levers, handle screws, locks etc.) are open, the
product/accessory can be moved.
Before opening the locking elements, hold the individual items firmly. After every
adjustment procedure, ensure that all locking elements are closed.
WARN IN G !
Risk of injury!
Products / accessories not attached properly may loosen and cause injuries.
Ensure that products / accessories are mounted correctly and that the securing
elements (handle screws, catches, levers, etc.) are closed and firmly tightened,
also ensure that moving parts are correctly secured.
7200.01XX
26 / 150 IFU 7200.01 EN 11
Safety notes
Safety notes for the OR table 2
2.2 Safety notes for the OR table
DA NG ER !
Risk of explosion!
When connected to the power supply the OR table is not authorised for use
in explosion prone AP-M areas.
An explosion could occur when using disinfectants or cleaning agents con-
taining alcohol, or flammable anaesthetics which are blended with air, oxy-
gen or nitrous oxide.
When operating on the mains supply, never use disinfectants, cleaning agents con-
taining alcohol, or flammable anaesthetics which are blended with air, oxygen or ni-
trous oxide!
DA NG ER !
Potentially fatal!
Electrical shock caused by increased leakage currents.
The patient may not touch the components that have not been defined as applied
part.
WARN ING !
Risk of injury due to material failure!
Loading may not exceed the permissible 454 kg total.
WARN ING !
Risk of infection!
If the operating table is used in areas with varying hygienic requirements,
there is a risk of infection.
Treat the operating table in accordance with the hygiene guideline and the instruc-
tions given in the chapter "Cleaning and disinfection".
WARN ING !
Risk of injury due to the operating table tipping!
If the OR table is not locked during patient transfer, the OR table may tip.
Always lock the OR table prior to transferring the patient [LOCK].
WARN ING !
Risk of injury caused by tipping of OR table!
The OR table may tip over if the patient is transferred over the head side of
the OR table.
Always transfer the patient to the OR table from the side.
WARN ING !
Risk of tilt!
The mobile operating table may tilt when crossing thresholds.
Do not cross thresholds with the mobile operating table.
WARN ING !
Risk of tipping!
If the patient is positioned incorrectly, the OR table may tip over.
Observe the prescribed patient orientation.
Do not position the patient with their torso on the leg plates.
7200.01XX
IFU 7200.01 EN 11 27 / 150
Safety notes
2 Safety notes for the OR table
WARN IN G !
Risk of injury due to the OR table tipping!
As of an overall load of the OR table of 250 kg, do not extend the swivel castors
[UNLOCK] and do not move the OR table.
WARN IN G !
Risk of injury!
Park the mobile operating table on level ground and secure with the [LOCK] func-
tion before each application and after each movement.
WARN IN G !
Risk of injury!
The OR table must be immobilised when a patient is being operated upon.
WARN IN G !
Risk of injury!
Whenever the product is mounted and adjusted, there is a danger of pinching
and shearing to the staff, patient and accessories.
Always ensure that no one can be subjected to pinching or shearing action or in-
jured in any other way and that the accessories do not collide with any nearby ob-
jects.
WARN IN G !
Risk of injury!
When setting down the OR table, there is a risk of crushing and shearing to
the feet or objects.
Before putting down the OR table, make sure there are no objects located under
the OR table base. When lowering the OR table, keep sufficient distance to the OR
table base.
CA UTIO N !
Property damage!
When tilting or sloping the table top or when articulating the leg or back plate, en-
sure that the table top, leg or back plate do not collide with either the column or the
operating table base.
CA UTIO N !
Property damage!
Any objects left on the base of the OR table will damage the casing as it
moves.
Do not put any objects on the OR table base.
CA UTIO N !
Property damages caused as a result of collision when moving/adjusting the
mobile operating table!
Remove potential hindrances before moving / adjusting the mobile operating table
and avoid collisions.
7200.01XX
28 / 150 IFU 7200.01 EN 11
Safety notes
Safety notes regarding the use of accessories 2
2.3 Safety notes regarding the use of accessories
DA NG ER !
Potentially fatal!
Patient may be endangered as a result of incorrect use.
Follow the instructions for use for all accessories.
WARN ING !
Risk of injury!
Accessories that are not approved by Maquet for this product, as well as ac-
cessories from other manufacturers, may cause injuries.
Only use Maquet accessories that have been approved for the product.
Accessories made by other manufacturers may only be used after obtaining written
permission from Maquet.
WARN ING !
Risk of injury due to material failure or tipping of the OR table!
The accessories mounted to the OR table may not exceed the maximum pro-
jection.
Accessories may be used within the permissible projection [8 Page 116] and tak-
ing into account the total load. Please observe these specifications when position-
ing the patient.
WARN ING !
The side rail accessory weight may not exceed 20 kg.
The maximum permissible overall load is reduced in accordance with the weight of
the attached accessories. Do not use accessories with higher weights.
CA UTI ON !
Property damage!
Side rail accessories with long lever arms may damage the product.
Do not use accessories with long lever arms.
CA UTI ON !
Property damage!
If accessories attached to the side rail protrude over the sides of the side rail
in the joint area, the accessory may collide with the table top when the joint
is adjusted.
When mounting the accessories, make sure that the accessories do not protrude
over the sides of the side rail in the joint area.
7200.01XX
IFU 7200.01 EN 11 29 / 150
Safety notes
2 Safety notes regarding service
2.4 Safety notes regarding service
DA NG ER !
Potentially fatal!
Electric shock!
Before opening the housing: Separate the product from mains voltage.
DA NG ER !
Potentially fatal!
The OR table may only be commissioned by a Getinge authorised service techni-
cian.
DA NG ER !
Potentially fatal!
The inspection of the OR table may only be carried out by qualified personnel who
ensure that the safety checks are carried out properly based on their training,
knowledge and experience gained through practical activities.
Technical information for carrying out the inspection is available from Getinge on
request.
WARN IN G !
Risk of injury!
Improper assembly, installation, expansion, adjustment, modification, re-
placement of hard-wired mains connections, maintenance and repair by un-
trained service personnel.
Assembly, installation, expansion, adjustment, modification, replacement of hard-
wired power cords, maintenance and repair may only be performed by Getinge-au-
thorised service technicians.
WARN IN G !
Risk of injury!
Functional restrictions to the product may be caused as a result of service
and maintenance work.
Do not carry out service and maintenance work to the product during an operation.
CA UTIO N !
Property damage!
If original Getinge spare parts are not used, the OR table may emit more interfer-
ence or be less immune to interference.
7200.01XX
30 / 150 IFU 7200.01 EN 11
Safety notes
Safety notes regarding padding 2
2.5 Safety notes regarding padding
DA NG ER !
The patient may slip off the OR table if the SFC pad is not secured properly
to the surface.
Do not use SFC pads for which the loop tape does not match up with the hook tape
on the product.
Only mount SFC pads to the product that have been approved for use with the
product.
DA NG ER !
The patient may slip off the OR table if the SFC pad is not secured properly.
Worn or wet loop tapes do not provide the SFC pad with hold on the product.
When attaching the SFC pad, check to ensure that it is properly secured.
WARN ING !
Health risk!
For health reasons, the pads must be covered with drapes.
CA UTI ON !
Improper use can cause property damage!
Use both hands to remove the padding.
CA UTI ON !
Property damage!
The pad can be damaged.
Do not place pointed or sharp objects on the pad.
Do not place the pad on pointed or sharp-edged surfaces nor pull over such.
CA UTI ON !
Property damage!
Pad may be deformed as a result of improper storage!
Pad should only be stored lying down and at room temperature.
7200.01XX
IFU 7200.01 EN 11 31 / 150
Safety notes
2 Safety notes EMC
2.6 Safety notes EMC
WARN IN G !
Hazard of injury!
Emission of electromagnetic signals of electrical units that are located near
the product or directly attached to the
product may have a negative impact on the functions of the product.
Do not place other electrical units near the product or directly at or on the product.
If this cannot be avoided, the product and the electrical units must be monitored
and checked for functional problems.
WARN IN G !
Hazard of injury!
Emission of electromagnetic signals by mobile RF communication appli-
ances (e.g. Mobile phones and transceivers) that are located near the product
may have a negative impact on the functions of the product.
Ensure that RF communication units (including cable-connected control panels and
the connection cables) are placed at a distance of at least 30 cm to the product.
WARN IN G !
Risk of injury!
In the vicinity of the product, accessories or cables that have not been spe-
cified or supplied by Getinge may, by way of reinforced electromagnetic radi-
ation or reduced electromagnetic resistance, influence the functions of the
product.
Only use cables supplied or specified by Getinge for use with this product.
Do not use any other accessories or cables not specified by Getinge.
7200.01XX
32 / 150 IFU 7200.01 EN 11
Initial operation
Storage 3
3 Initial operation
3.1 Storage
• Packaged OR table components may be stored under the named environmental conditions
for up to 15 weeks [8 Page 135]. In order to prevent a rechargeable battery defect, the bat-
tery must be recharged after this time has passed.
• When transporting and storing, do not drop the OR table, lay it down, or place it upside down.
• When transporting and storing, protect the OR table from moisture.
• If a battery-operated device is to be stored or transported for longer than 4 weeks, the battery
must be recharged before using.
• Observe the notes on the packaging.
3.2 Ambient conditions
NO TE
Conduction by way of conductive pad to the metal parts of the OR table is de-
signed to provide protection against electro-static charging. The OR table is con-
nected via the equipotential bonding connection to the equipotential bonding of the
operating room.
• The anti-static properties are dependent on the supplied pads.

• "AP" protection requires an electrically conductive path on a conductive floor.
• Electrical ballasts and dimmers may interfere with the IR remote control.
3.3 Power supply

• Charge the mobile OR table fully before using it for the first time.
• The battery integrated in the base supplies the OR table with an operating voltage of
DC 24 V. The supply voltage is specified on the type plate. If the supply voltage deviates from
this value, it must be reset on the OR table and the specification must be changed on the
type plate accordingly.
7200.01XX
IFU 7200.01 EN 11 33 / 150
Initial operation
3 Connecting the service interface
3.4 Connecting the service interface
DA NG ER !
Risk of explosion caused by sparks!
When plugging and unplugging the plug to the service interface, there is a
risk of explosion caused by sparks.
The plug may not be plugged into or removed from the service interface during OR
operation.
WARN IN G !
Risk of injury!
Risk of stumbling as a result of loosely laid cables.
Fix the cable properly when laying.
CA UTIO N !
Property damage!
The cable of the control device may be damaged during adjustment proced-
ures.
Make sure that the cable is not crushed, trapped or damaged in any other way.
The connection for the service interface is loc-

ated on the upper column cladding.
1. Loosen the screw 1 with the Allen key.
2. Remove the cover 2 .
Fig. 10: Removing the cover
7200.01XX
34 / 150 IFU 7200.01 EN 11
Initial operation
Connecting the service interface 3
3. Press cable 3 firmly into the service inter-

face connector.
Ø Check seating of the cable to ensure it
is secure.
Fig. 11: Connecting the service interface
7200.01XX
IFU 7200.01 EN 11 35 / 150
Initial operation
3 IR code
3.5 IR code
3.5.1 Grouping of IR codes according to product groups
WARN IN G !
Risk of injury caused by unintentional movement of the OR table!
If two OR tables within a product group have the same IR code, the operation
with the control device may result in unintentional movement of the second
OR table.
Ensure that IR codes are assigned only once within a product group.
The OR table and control device must be set to the same IR code. The IR code has two charac-
ters and is made up of the numbers 0–9 and the letters A–F. The factory set IR code for the con-
trol device is [0 0]. For this reason, this IR code may never be used as the IR code. If multiple OR
tables of the same product group are used on the same floor, you must ensure that these OR
tables do not use the same IR code.
The following products are summarised into product groups in order to ensure fault-free parallel
operation:
• Operating table system 1120, BETAMAQUET 1140
• OR tables HEIDELBERGER 1130, BETASTAR 1131.01/02, 1211 (gynaecology/urology),
1223 (ENT/head), ORTHOSTAR 1420, ORTHOSTAR II 1425, ENDOSTAR 1532/1533
• Patient transfer units 1952, 1954, 1973, 1974
• ALPHAMAQUET 1150 operating table system
• OTESUS 1160 operating table system
• MAGNUS 1180 operating table system
• Operating table system AWIGS / VIWAS
• OR tables BETACLASSIC 1118.01, ALPHACLASSIC 1118.02/03, ALPHACLASSIC PRO
1118.06
• OR table BETASTAR 1131.12
• OR tables ALPHASTAR 1132.11, ALPHASTAR PLUS 1132.13, ALPHASTAR PRO
1132.21/22
• ALPHASTAR TOP 1132.17 OR table
• ALPHAMAXX 1133 OR table
• YUNO 1433 OR table
• OP-Tisch MEERA CL 7000, MEERA ST 7100, MEERA 7200
7200.01XX
36 / 150 IFU 7200.01 EN 11
Initial operation
Venting the hydraulic oil 3
3.5.2 Determining / specifying the IR code

1. Read the IR code at the OR table (corded hand control or label).
2. Read the IR code at the IR remote control (menu or label).
3. Check whether this IR code is being used by another OR table.
If the preset IR code is not being used by another OR table:

1. Set the IR code for IR remote control in the [Service] menu of the IR remote control to the IR
code of the OR table .
2. Perform a functional test [8 Page 37].
If the preset IR code is already being used by another OR table:

1. Specify a new IR code and make a note of it here:
Code 1: Code 2:
1. Set the IR code for the OR table in the [Service] menu of the corded hand control .
2. Set the IR code for the IR remote control in the [Service] menu of the IR remote control .
3. Perform a functional test [8 Page 37].
3.5.3 Carrying out a functional test

1. Press any button.
Ø The IR remote control and the OR table switch themselves on.
2. Press and hold any button.
Ø The OR table executes the selected function.
3.6 Venting the hydraulic oil

Air bubbles may form in the hydraulic oil during shipping.
1. Adjust the mobile operating table in all directions until the end positions are reached.
Ø The air bubbles will dissolve.
7200.01XX
IFU 7200.01 EN 11 37 / 150
Hand controls and functions
4 Overview of control devices
4 Hand controls and functions
4.1 Overview of control devices

The OR table can be power-adjusted using the following control devices:
• Universal control device (1009.25A0)
• Corded control device (7200.90A0)
• IR remote control (7200.91A0)
• Foot switch (1009.81J0/J1/J2)
• Override control panel on the column (integrated into the column)
Control device – Notes on use:
• As a general principle, do not perform adjustments with two control devices at the same time.
In the event that multiple control devices are accidentally used simultaneously, the override
control panel and corded controls (e.g. corded control device) take priority over the infrared
devices (IR remote control). If equally ranked control devices are used at the same time, ad-
justment may be interrupted or stopped.
• The adjustment speed may be modified according to the overall load and protrusion.
In the event of large overall loads/protrusion, the speed of lowering actions is increased and
the speed of raising actions is reduced.
• The OR table can only be adjusted without restrictions with retracted swivel castors (LOCK
function is activated) [8 Page 76].
If the swivel castors are extended (UNLOCK function is activated), the following adjustment
functions are released: Inclination, back and leg plates, zero position, OR table down, change
of patient orientation and lifting of lateral tilt. The adjustment functions, OR table up and Pa-
tient lateral tilt as well as the saved patient positions are all blocked.
• Carry out the adjustment functions of the operating table only with the castors locked (LOCK).
If an adjustment function is performed without locking the castors (UNLOCK), a message ap-
pears on the display of the control unit indicating that the castors must be locked.
7200.01XX
38 / 150 IFU 7200.01 EN 11
Mounting the control device to the side rail 4
4.2 Mounting the control device to the side rail
CA UTI ON !
Property damage!
A control unit attached to the side rail can slip off the side rail when the table
top is adjusted or cause collisions with the OR table or other accessories.
Remove the control device from the side rail before adjusting the table top.
1. Attach the bracket 1 to the side rail 2 .
1
2
Fig. 12: Mounting the control device to the side

rail
4.3 Override control panel

The mobile operating table is fitted with an override control panel for emergency operation. If
there are any malfunctions or if the control device is defective, then the mobile operating table
can be controlled using the override control panel.
The override control panel is located on the upper column casing.
Notes on the use of the override control panel:
• When operating the OR table using the override control panel, the collision warning function
is not active. Watch every adjustment carefully and avoid collisions, especially when imple-
menting extreme inclination and lateral tilt settings.
• When the rechargeable battery of the OR table is empty, the override control panel only func-
tions if the OR table is connected to the power supply. In this case, the OR table may not be
used in (AP-M) areas prone to explosion.
• The status display is only active when the OR table is switched on.
• To execute an adjustment, press the [ON] button and the appropriate adjustment button at
the same time, and hold down until the desired position has been reached.
• When operating using the override control panel, the NORMAL/REVERSE patient orientation
is not effective. During adjustment procedures pay attention to the long and short segment of
the OR table base.
7200.01XX
IFU 7200.01 EN 11 39 / 150
4 Override control panel
4.3.1 Control buttons and functions
2 3 4 5 6 7 8 9 10 11
LOCK UNLOCK TREND. UP REV.
UP
1 12
DOWN
13
L-SHIFT
TILT TILT
ON DOWN
19 18 17 16 15 14
Fig. 13: Override control panel
1 Status display: LED mains operation 11 [UP] Leg plate up*

[8 Tab. 8 Page 72] 12 [DOWN] Leg plate down*
2 Status display: LED battery charge status 13 [DOWN] Back plate down*
[8 Page 73]
14 [L-SHIFT] Longitudinal shift in the direction of
3 Status display: LED LOCK (green) the REVERSE mounting point
[8 Page 77]
15 [L-SHIFT] Longitudinal shift in the direction of
4 [LOCK] OR table is locked* the NORMAL mounting point
5 Status display: LED UNLOCK (orange) 16 [TILT] Lateral tilt to right*
[8 Page 77]
17 [DOWN] OR table down
6 [UNLOCK] OR table can be moved*
18 [TILT] Lateral tilt to left*
7 [TREND.] Trendelenburg*
19 [ON] Switches the motor on. Must be
8 [UP] OR table up pressed in addition to any function button.
9 [REV.] Reverse Trendelenburg*
10 [UP] Back plate down*
*Button assignments and functions correspond to operation with a NORMAL patient orientation.
7200.01XX
40 / 150 IFU 7200.01 EN 11
Corded hand controls 4
4.4 Corded hand controls
4.4.1 Connecting/removing corded control devices
CA UTI ON !
Property damage!
The cable of the control device may be damaged during adjustment proced-
ures.
Make sure that the cable is not crushed, trapped or damaged in any other way.
The control device sockets for the cable control unit and foot switch are located on the upper
column cladding.
Connecting a corded control device

1. Open the cover 1 of the socket for control
devices.
2. Insert the plug 2 into the socket for con-
trol devices.
3. Ensure that the plug is properly seated.
Ø The corded control device is ready for
1 use.
Disconnecting a corded control device

1. Remove the plug from the socket for con-
2 trol devices.
Fig. 14: Connecting corded control devices
7200.01XX
IFU 7200.01 EN 11 41 / 150
4 Corded hand controls
4.4.2 Foot switch (1009.81J0/J1/J2)
NO TE
The control function "operating table lock " cannot be cancelled with the foot
switch.
The foot switch (1009.81J0/J1/J2) is connected to the column [8 Page 41]. Rocker switches 1
to 4 have the same functions for all versions of the foot switch. Rocker switches 5 and 6 have
different functions.
Rocker switches 1 to 4
1. Table top up
2. Table top down
3. Reverse Trendelenburg (inclination foot
down)
4. Trendelenburg (inclination head down)
Rocker switch 5
• Foot switch version (1009.81J0):
Back plate up
1 Lateral tilt left
2
3 • Foot switch version (1009.81J2):
4
5 Leg plate up
6
Rocker switch 6
Back plate down
Fig. 15: Foot switch
Lateral tilt right
Leg plate down
7200.01XX
42 / 150 IFU 7200.01 EN 11
Universal control device (1009.25A0) 4
4.5 Universal control device (1009.25A0)
4.5.1 Notes on use
NO TE
The graphics in these instructions for use show the available functions of the
touchscreen user interfaces. Depending on the OR table being operated, there
may be differences between the user interface described here and the actual user
interface.
Control device – Notes on use:

• On every occasion, before adjusting the OR table, check the set patient orientation
[8 Page 14] and adapt as necessary.
• As a general principle, do not perform adjustments with two control devices at the same time.
In the event that multiple control devices are accidentally used simultaneously, the override
control panel and corded controls (e.g. corded control device) take priority over the infrared
devices (IR remote control). If equally ranked control devices are used at the same time, ad-
justment may be interrupted or stopped.
• The adjustment speed may be modified according to the overall load and protrusion.
In the event of large overall loads/protrusion, the speed of lowering actions is increased and
the speed of raising actions is reduced.
• The adjustment functions are executed for as long as the appropriate adjustment button is
pressed. If the adjustment button is released, the adjustment is stopped.
Operating instructions control device as IR remote control:

• The capacity of a fully charged rechargeable battery is sufficient for several days of OR oper-
ation or around 2.5 hours of continuous operation.
• In order to avoid empty batteries of the control device during surgery, we recommend storing
the operating device in the charging cradle when not in use.
• When the battery charge is ≤20 %, the touchscreen shows the message Battery low for ap-
proximately 5 seconds. The control device remains switched on and can be used again.
• When the battery charge is ≤5 %, the touchscreen shows the message Battery empty. The
control device switches itself off after 5 seconds. After 10 seconds in the charger cradle, the
control device can be switched back on and you can continue to use it in the charger cradle.
Operating instructions control device as corded control device:

• If the control device is used as a corded control device for an extended period of time, the
battery of the control device will not be charged during this period. The battery of the control
unit is either not fully charged or empty.
7200.01XX
IFU 7200.01 EN 11 43 / 150
4 Universal control device (1009.25A0)
4.5.2 Acoustic signals of the control device
Acknowledgement tone
▪ The acknowledgement tone is emitted
once, when a button is pressed.
Quick acoustic signal (4 acoustic signals
per second)
▪ 4 quick acoustic signals will sound if a
button is not pressed correctly. Then the
control device will switch off.
Tab. 5: Acoustic signals
4.5.3 Button assignment and functions
NO TE
Buttons light up for active functions.
1 [Green up] button

2 [Blue up] button
3 [Blue down] button
4 [Green down] button
5 Multifunctional button left
6 [Trendelenburg]* button
7 [Table top up] button
8 [Lateral tilt left]* button
1 10 9 Button [Stand-by]
2
10 [Magenta up] button
11
3 11 [Magenta down] button
12 Multifunctional button up
12
4 13 Multifunctional button right
13
14 Multifunctional button down
5 14 15 [Foot down inclination]* button
6 15 16 [Lateral tilt right]* button
16 17 [Table top down] button
7
18 [Zero.position] button
8 17
19 [UNLOCK] button / Lock Menu quick access
18 menu
9
19 *Button assignments and functions correspond
to operation with a NORMAL patient orienta-
tion.
Fig. 16: Button assignment and functions of the
control device
7200.01XX
44 / 150 IFU 7200.01 EN 11
Adjustment functions 4
4.6 Adjustment functions
NO TE
If a patient is on the OR table:Secure the patient prior to moving / adjusting the OR
table.
4.6.1 Adjusting the height of the OR table
Lowering the OR table

1. Push and hold the [Down] 1 button.
Ø The OR table moves down.
Lifting the OR table

1. Push and hold the [Up] 2 button.
Ø The OR table moves up.
2
Fig. 17: Lifting / lowering the OR table
4.6.2 Adjusting the back plate
Raise the back plate

1. Push and hold the [Blue up] 1 button.
Ø The back plate is adjusted upwards.
Ø The adjustment angle is displayed on
1 the touchscreen.
Lowering the back plate

1. Push and hold the [Blue down] 2 button.
Ø The back plate is adjusted downwards.
2 the touchscreen.
Fig. 18: Adjusting the back plate
7200.01XX
IFU 7200.01 EN 11 45 / 150
4 Adjustment functions
4.6.3 Adjusting the leg plates
Raising the leg plates

1. Push and hold the [Magenta up] 1 button.
Ø The leg plates are adjusted upward.
the touchscreen.
1
Lowering the leg plates
1. Push and hold the [Magenta down] 2 but-
ton.
Ø The leg plates are adjusted downward.
2 Ø The adjustment angle is displayed on
the touchscreen.
Fig. 19: Adjusting the leg plates
7200.01XX
46 / 150 IFU 7200.01 EN 11
4.6.4 Balancing the leg plate

Adjustments of the REVERSE (leg plate) mounting point may, over time, result in a slight offset.
At regular intervals, align the leg plates or the one-section accessory using the [0-position] button
and the [Magenta up] button in order to correct any offset.
Prerequisites:
• The patient is not lying on the OR table.
• The OR table has been set to the NOR-
1 MAL patient orientation.
1. Press the [Magenta up] button 1 and
move the leg plates to the uppermost posi-
tion.
2. Press the [Magenta up] button 1 in con-
2
junction with the [0-position] button 2 and
hold for at least 10 seconds.
Ø The balancing process is executed and
can be recognised both by the audible
cracking sound and the small visual
motions of the leg plates.
Fig. 20: Balancing the leg plate Ø The balancing process is complete
when the operating note End position
achieved! is shown on the display.
3. If necessary, the balancing process may
be repeated after 5 seconds.
Fig. 21: Balancing the leg plate
7200.01XX
IFU 7200.01 EN 11 47 / 150
4.6.5 Inclining the table top
WARN IN G !
Risk of injury!
If the patient is not secured during positioning, when adjusting the OR table
or when positioning the patient (particularly when the inclination and/or tilt
features are used), then the patient could slip off the table top in an uncon-
trolled manner or their legs and arms may hang down.
observation.
Tilt table top into Trendelenburg position

1. Push and hold the [Trendelenburg] button.
Ø The table top will be set to the Trendelenburg position.

Ø The current adjustment angle is shown on the touchscreen.
Ø When the end position is reached, this is indicated on the touchscreen and a signal is
sounded on the column.
Tilt table top into reverse Trendelenburg position

1. Push and hold the [Reverse Trendelenburg] button.
Ø The table top will be set to the reverse Trendelenburg position.

Ø The current adjustment angle is shown on the touchscreen.
Ø When the end position is reached, this is indicated on the touchscreen and a signal is
sounded on the column.
7200.01XX
48 / 150 IFU 7200.01 EN 11
4.6.6 Tilting the table top laterally
WARN ING !
Risk of injury!
If the patient is not secured, particularly when adjusting/moving, the patient
and/or their extremities may slip in an uncontrolled manner.
observation.
Lateral tilt, left / right

1. Press and hold the [Lateral tilt, left] 1 or
[Lateral tilt, right] 2 button.
Ø The table top moves accordingly about
the head-foot axis to the right or left .
Ø The current adjustment angle is shown
2 on the touchscreen.
1
Ø Depending on the connected OR table,
the message "Extreme lateral tilt" is dis-
played on the touchscreen.
Fig. 22: Tilting the table top laterally
7200.01XX
IFU 7200.01 EN 11 49 / 150
4.6.7 Moving the table top longitudinally
NO TE
The longitudinal shift of the table top is stopped for approximately 0.5 seconds
once the CENTRAL position is reached and a short acoustic signal sounds. Then
the lateral shift will be continued past the centre position.
NO TE
The longitudinal shift can slow down or stop at a high inclination and simultan-
eously high overall load.
If necessary reduce the inclination in order to carry out longitudinal shift.
Moving the table top longitudinally

1. Depending on the desired direction, press
and hold one of the two buttons for longit-
udinal shift.
Ø The table top moves in the selected dir-
ection.
Ø When the end position is reached, this
is indicated on the display and a signal
is sounded.
Fig. 23: Moving the table top longitudinally
7200.01XX
50 / 150 IFU 7200.01 EN 11
4.6.8 Moving the table top to the horizontal position
WARN ING !
Risk of injury!
When aligning the leg plate and especially when using knee crutches, the pa-
tient may be injured.
Check the patient's position and support when aligning the leg plate and adapt it, if
necessary.
NO TE
The manual adjustment functions of the accessories (head and leg plates) will not
be equalised.
1. Press the [zero-position] button and hold it as long as you wish to execute this function.
Ø Lateral tilt is reset.

Ø Inclination will be lifted and the back plate will be aligned.
The adjustments of back plate and inclination will be executed alternately.
Ø When the final position is reached this is shown on the display and a signal will sound.
Ø For safety reasons, the leg plate and / or the leg holders are not yet aligned.
2. Release the [zero-position] button.
3. Check the patient's position and adapt it, if necessary.
4. Press the [zero-position] button again and hold it as long as you wish to execute this function.
Ø The leg plate is aligned.

Ø The table top is aligned horizontally.
Ø When the final position is reached this is shown on the display and a signal will sound.
5. Release the [zero-position] button.
7200.01XX
IFU 7200.01 EN 11 51 / 150
4 Operating menu
4.6.9 Deactivating the lock function temporarily
Prerequisites:
• OR table or table top adjustment functions
are locked [8 Page 68].
Deactivating the lock function temporarily

1. Press the button [Table top down] 1 and
the button [Table top up] 2 at the same
2
time for at least one second.
Ø The locking function is disabled until the
1 system is switched off again.
Fig. 24: Deactivating the lock function temporar-

ily
4.7 Operating menu
4.7.1 Display start screen
NO TE
The battery charge level of the control device is displayed in the status bar.
The battery charge level of the currently connected OR table is displayed in the
main window below the OR table graphic.
2
OR01-14 The start display on the touchscreen is divided
1 into different areas with different icons:
PATIENT POSITIONS MENU
3 4 5 1 Status bar area [8 Page 53]
6
2 Connection active
7 3 Display of the name of the operating table and
IR code of the connected operating table
4 External power supply of the control device
5 Battery symbol of the control device
6 Navigation bar or operating bar
7 Mainscreen area
8 External power supply of the operating table
with mobile/independently manoeuvrable
column
8 9 9 Battery symbol of the operating table with mo-
bile/independently manoeuvrable column
PATIENT
10 ORIENTATION 10 Control bar area (optional)
Fig. 25: Display start screen
7200.01XX
52 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.2 Symbols for status bar
Symbol Meaning
control device receives signal from the operating table.
Control device is connected to external power supply (charger or cable).
Battery of the control device is fully charged.
The battery charge level of the control unit is in the range of approx. 83 %. The
battery charge capacity is sufficient.
battery charge capacity is sufficient.
battery charge capacity is sufficient for one surgery.
battery must be charged soon.
battery must be charged soon.
Battery of the control device is nearly fully charged. The battery must be charged.
Tab. 6: Symbols for status bar
7200.01XX
IFU 7200.01 EN 11 53 / 150
4 Operating menu
4.7.3 Main menu [Menu]
OR01-14 The following functions and settings may be

selected in the MENU main menu:
1 Menu OR Table Connection [8 Page 54]
1 2 MENU 3 2 Menu Lock Menu
OR Table OR Table
3 Menu OR Table Settings
Lock Menu
Connection Settings 4 Menu Device Settings [8 Page 58]
5 Drive menu
Device
Drive
Active Cable 6 Active Cable Charging menu
Settings Charging
4 5 6
Fig. 26: Overview of main menu
4.7.4 Connect the OR table

The control device can be connected to an operating table in several ways:
• Direct connection with a cable to the operating table. The operating table is automatically
connected to the control device as soon as a button on the control device is pressed.
• Connection to the operating table via an IR code. The connection with an IR code can be es-
tablished via the OR Table Connection menu.
OR01-14 The following functions and settings can be

selected in the OR Table Connection menu:
BACK
1 Connect to OR table menu item
OR TABLE CONNECTION
▪ Connect to new OR table
1 Connect to OR table ▪ Last connections
2 2 Disconnect from OR table menu item
Disconnect from OR table
3 Rename OR table menu item
3 Rename OR table 4 View IR code menu item
4 View IR code
Fig. 27: Menu OR Table Connection
7200.01XX
54 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.4.1 Connecting a new OR table
OR01-14 Prerequisites:
BACK • The OR Table Connection menu is open.
OR TABLE CONNECTION Connect the operating table

1 Connect to new OR table
1. Touch the Connect to OR table button.
Last connections
Ø Known operating tables are listed and
the menu item Connect to new OR
14 - OR-01
table is displayed.
15 - OR-02 2. Touch the Connect to new OR table but-
ton 1 .
Ø The window for entering the IR code
appears.
Fig. 28: Connecting a new OR table
OR01-14 Enter IR code

CANCEL OK 1. Enter the IR code of the new operating
1 table.
IR-CODE
2. Touch the OK button 1 .
Enter IR code Ø The control device searches for avail-
able product groups within the trans-
mission range.
0 1 2 3 3. Touch the OK 1 button.
Ø A new operating table is connected.
4 5 6 7
8 9 A B
C D E F
Fig. 29: Enter IR code
7200.01XX
IFU 7200.01 EN 11 55 / 150
4 Operating menu
4.7.4.2 Reconnecting the known OR table
BACK • The OR Table Connection menu is
OR TABLE CONNECTION
opened.
1. Touch the Connect to OR table button.
Connect to new OR table
Last connections
Ø Known operating tables are listed and
the menu item Connect to new OR
14 - OR-01
table is displayed.
15 - OR-02 2. Touch already known operating table from
the list.
Ø Operating table is connected.
Ø The OR Table Connection menu is
opened.
Fig. 30: Connecting a known OR table
4.7.4.3 OR table is renamed
CANCEL OK • The OR Table Connection menu is
1
opened.
OR TABLE NAME
Enter OR table name 1. Touch the Rename OR table button.
OR-01:
Ø Window with operating table name and
virtual keyboard is displayed.
q w e r t z u i o p 2. Enter the name of the operating table.
a s d f g h j k l
Ø Operating table has been renamed.
y x c v b n m
123 ...
Fig. 31: OR table is renamed
7200.01XX
56 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.4.4 Disconnect the OR table
CANCEL • The OR Table Connection menu is
opened.
Disconnect from OR table
1. Touch the Disconnect from OR table
Remote connected to
button.
OR-01 14
IR code: 14 Ø Window with connected table and asso-
ciated IR code is displayed.
2. Touch the DISCONNECT button 1 .
Ø Operating table is disconnected.
1
DISCONNECT
Fig. 32: Disconnect the OR table
4.7.4.5 Show IR code
BACK • The OR Table Connection menu is
opened.
View IR code
1. Touch the View IR code button.
Remote connected to
OR-01 14
Ø Window with connected table and asso-
IR code: 14 ciated IR code is displayed.
Connect to new OR table
Fig. 33: Show IR code
7200.01XX
IFU 7200.01 EN 11 57 / 150
4 Operating menu
4.7.5 Menu [Device Settings]
4.7.5.1 Set the brightness on the touchscreen
NO TE
The control device is equipped with a sensor for automatic brightness control on
the right above the touchscreen. Depending on the ambient brightness, the illumin-
ation of the touchscreen and the keyboard is adjusted.
CANCEL OK • The Device Settings menu is open.
DEVICE SETTINGS 1. Touch the slider and move it to the right to
increase the brightness, or move it to the
Brightness
left to reduce the brightness.
Language English
2. Touch the OK button.
Reset Ø Brightness is set.
Log files
Date / Time
System information
Sleep Mode
Fig. 34: Adjusting brightness
4.7.5.2 Set the language
1
LANGUAGE 1. Touch the Language button.
English Ø A window with all available languages
is displayed.
Deutsch
2. Touch the desired language.
Ø The status display next to the selected
language lights orange.
Ø The Device Settings menu is dis-
played.
Ø The selected language is set.
Fig. 35: Set the language
7200.01XX
58 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.5.3 Resetting the control device

When resetting to factory settings, all data entered by the user is deleted, and the device is reset
to factory settings. The connection to the operating table is deleted and must be re-established
for the operating table to be able to be activated once again using the control device.
DEVICE SETTINGS 1. Touch the Reset button 1 .
Brightness Ø Window with query is shown.
Language English
1 Ø The control device is reset to factory

Reset
settings.
Log files
Date / Time
System information
Sleep Mode
Fig. 36: Resetting the control device
7200.01XX
IFU 7200.01 EN 11 59 / 150
4 Operating menu
4.7.5.4 Calling up system information

System information can be called via the menu item System information.
BACK • The Device Settings menu is open.
SYSTEM INFORMATION 1. Touch the System information button.
GUI version: 0.0.0

Ø System information (e.g. software ver-
COM version: 0.0.0 sion) are shown.
StatTxOk: 0 Err: 0
StatRxOk: 0 Err: 0
StatCrcErr: 0
HW-ID Main: 0 IR: 0 KEY: 0 LCD: 0
Date / Time: 2010-01-01-00-00
Bat. t2empty: 0 min, SoH: 0 %
Bat. pcharge: 0 mAh, cycle count: 0
Fig. 37: Calling up system information
7200.01XX
60 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.6 Set the patient orientation
NO TE
Regardless of the set patient orientation, the displayed patient head on the control
device is always on the left side of the OR table in the blue area on the touch-
screen.
NO TE
The currently set configuration is highlighted in orange on the touchscreen and
marked with (active).
BACK • The start screen is opened.
PATIENT ORIENTATION 1. Check patient orientation from the cur-
rently connected operating table. Please
Observe blue dot position!
refer to the definition of the patient orienta-
1
Patient orientation tion in the respective operating table in-
NORMAL
(active) structions.
2. Touch the PATIENT ORIENTATION but-
Patient orientation
REVERSE ton.
Ø The window for setting the patient ori-
entation is displayed.
3. Touch the Patient orientation NORMAL
button 1 .
- or -
Fig. 38: Setting NORMAL patient orientation touch the Patient orientation REVERSE
button 2 .
Ø Window with the query Patient
orientation correct? is shown.
Ø The selected patient orientation is set.
7200.01XX
IFU 7200.01 EN 11 61 / 150
4 Operating menu
OR01-14 Setting REVERSE patient orientation

BACK 1. Check patient orientation from the cur-
rently connected operating table. Please
PATIENT ORIENTATION
refer to the definition of the patient orienta-
Observe blue dot position! tion in the respective operating table in-
structions.
Patient orientation
NORMAL 2. Touch the PATIENT ORIENTATION but-
ton.
1 Patient orientation
REVERSE Ø The window for setting the patient ori-
(active)
entation is displayed.
3. Touch the Patient orientation REVERSE
button 1 .
Ø Window with the query Patient
orientation correct? is shown.
Fig. 39: Setting REVERSE patient orientation 4. Touch the OK button.
Ø REVERSE patient orientation is set.
7200.01XX
62 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.7 Select the preset patient position
WARN ING !
Risk of injury!
The use of the preset positioning position may cause undesired movements.
Always observe the patient's position and positioning when aligning the OR table
using preset positioning positions. If undesired movements occur, release the but-
ton and abort the selected patient positioning.
NO TE
The preset positions vary depending on the connected OR table. For the available
preset positions, refer to the OR table's instructions for use.
STORE NEW QUICK • Start screen is open.
POSITION MEMORY
1. Touch the PATIENT POSITIONS button.
PATIENT POSITIONS
Standard positions Ø The window with available patient posi-
BEACH CHAIR FLEX REFLEX
tions is shown.
2. Select the desired patient position.
BACK Ø The Move to position window and the
HORIZONTAL
following operating note are displayed.
Move to
Folder position
Folder01
3. To move to the selected patient position,

EDIT EDIT press the highlighted multifunction button
[Up] on the control device.
Fig. 40: Available patient positions
Ø The operating table is moved to the se-
lected patient position.
7200.01XX
IFU 7200.01 EN 11 63 / 150
4 Operating menu
4.7.8 User-defined patient positions

If the operating table is set to a certain position, this position can be saved in the Individual
positions list or in an individually created folder.
4.7.8.1 Save user-defined patient positions

Depending on the operating table used, several user-defined patient positions can be stored in
the control device. For further information, refer to the operating table operating instructions.
1
STORE NEW QUICK • The PATIENT POSITIONS menu is open.
POSITION MEMORY
1. Touch the STORE NEW POSITION button
PATIENT POSITIONS
1.
Standard positions

Ø The window for naming the new patient
position is opened.
BACK
2. Enter the name of the new patient posi-
HORIZONTAL tion.
Individual positions
Ø The new patient position is stored in the
Dr.Kruger_01
Individual positions list in the
PATIENT POSITIONS menu.
EDIT
Fig. 41: Save new position
7200.01XX
64 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.8.2 Selecting a user-defined patient position
POSITION MEMORY
1. In the menu PATIENT POSITIONS scroll
PATIENT POSITIONS
down and select the desired position from
Standard positions
the list Individual positions 1 .
Ø The MOVE TO POSITION window and
the following operating note are dis-
BACK
HORIZONTAL played.
Move to
1 position
Dr.Kruger_01
2. To move, press the marked button on the

EDIT
operating foil.
Ø Moves to selected patient position.
Fig. 42: Select position
OR01-14
BACK
MOVE TO POSITION
OR table will move to
position
Dr.Kruger_02.
Watch OR table!
Move to
position
Fig. 43: Moving to position
7200.01XX
IFU 7200.01 EN 11 65 / 150
4 Operating menu
4.7.8.3 Editing user-defined patient positions
POSITION MEMORY
PATIENT POSITIONS Editing a patient position from the

Standard positions Individual positions list
BEACH CHAIR FLEX REFLEX 1. Touch the EDIT 1 button.
Ø The list of saved positions is displayed.
BACK
HORIZONTAL 2. Select the desired position from the list.
Dr.Kruger_01
1
EDIT
Fig. 44: Menu PATIENT POSITIONS
OR01-14 3. To delete the position, touch the DELETE

BACK POSITION button 2 .
Ø The position is deleted.
EDIT INDIVIDUAL POSITION
Select position
4. To rename the position, touch the
RENAME POSITION button 3 .
0123456789ABCDE
Ø A window to rename the position
Dr.Kruger_01 opens.
5. Enter the new name of the position.
Dr.Kruger_02
Dr.Kruger_03
Ø Position is saved with a new name.
Dr.Schmidt_01
DELETE RENAME
2 POSITION POSITION 3
Fig. 45: Edit own positions
7200.01XX
66 / 150 IFU 7200.01 EN 11
Operating menu 4
4.7.8.4 Quick saving user-defined patient positions

In the quick-save mode of the control device, a patient position can be save without a name.
When saving another patient position in quick-save mode, the previously stored position is over-
written.
BACK
• The PATIENT POSITIONS menu is open.
QUICK MEMORY Quick saving patient positions

1 1. Touch the QUICK MEMORY button.
Store current OR table position
Ø The menu QUICK MEMORY is shown.
Move to quick memory position
2. Touch the Store current OR table
position 1 button.
Ø Query Store current OR table
position? is displayed.
TREND: 0° L: 0°
0°
TILT: 0° R: 0°
Fig. 46: Quick-saving a position
OR01-14 3. Touch the STORE POSITION 2 button.

BACK Ø The current patient position is stored in
the quick-save memory.
QUICK MEMORY
Store current OR table position?
TREND: 0° L: 0°
0°
TILT: 0° R: 0°
2
STORE POSITION
Fig. 47: Quick-saving a position
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IFU 7200.01 EN 11 67 / 150
4 Operating menu
4.7.8.5 Move to quick-save memory position
BACK
• The PATIENT POSITIONS menu is open.
1. Touch the QUICK MEMORY button.
QUICK MEMORY
Ø The menu QUICK MEMORY is shown.
Store current OR table position
2. Touch the Move to quick memory
1
Move to quick memory position position 1 button.
Ø The MOVE TO POSITION window and
the following operating note are dis-
played.
Move to
position
TREND: 0° L: 0°
0°
TILT: 0° R: 0°
3. Press the displayed multifunction button
[Up] on the control device.
Fig. 48: Move to quick-save memory position
Ø Moves to selected quick-save position.
4.7.9 OR table adjustment function or lock / unlock button
NO TE
The Lock Menu menu can be accessed via the touchscreen or the [UNLOCK] but-
ton.
With the operating table lock, the motorised adjustment functions of both the operating table
column and the table top are locked to prevent unintentional adjustment of the operating table
and the table top.
With the surgical table top lock, the motorised adjustment functions of the table top are locked to
prevent unintentional adjustment of the table top.
The status display lights up orange next to the activated lock.
NO TE
This menu shows whether the OR table is locked (Wheel Lock enabled) or mov-
able (Wheel Lock disabled).
7200.01XX
68 / 150 IFU 7200.01 EN 11
Operating menu 4
CANCEL OK
• The Lock Menu menu is open.
LOCK MENU Lock operating table/table top

1. Touch the Operating Table Lock button
Operating Table Lock
- or -
Table Top Lock touch the Table Top Lock button.
Wheel Lock disabled

Ø The status display is illuminated orange
depending on the lock selected.
Ø The selected lock is activated.
Ø Depending on the selected lock, the
Unlock message OR table lock active or OR
Lock table top lock active is displayed in
the start display of the touchscreen.
Fig. 49: Lock OR table / OR table top
Unlocking the operating table/table top
1. Touch the Operating Table Lock button
- or -
touch the Table Top Lock button.
Ø Status display is greyed out.
Ø Operating table lock or operating table
top lock is deactivated.
7200.01XX
IFU 7200.01 EN 11 69 / 150
Operation and use
5 General
5 Operation and use
5.1 General
The mobile table MEERA can be moved within the OR environment on casters. Versions
(7200.01B2/F2) are equipped with a motorised drive.
The OR table top is equipped with a motorised longitudinal shift and mounting points for motor-
ised adjustment of the bottom back plate (NORMAL mounting point) and leg plate (REVERSE
mounting point). Additional manually adjustable accessories may be mounted to the NORMAL
and REVERSE mounting points, as well as the side rails .
The OR table is power-adjusted using the following control devices:
• Corded control device, optional
• IR remote control, optional
• Foot switch, optional
• Override control panel
7200.01XX
70 / 150 IFU 7200.01 EN 11
Operation and use
OR table 5
5.2 OR table
5.2.1 Acoustic signals issued by the OR table

In certain situations, the OR table outputs acoustic signals.
Brief signal tone

A brief signal tone will sound in the following
cases:
▪ An operating message is shown on the
display of the hand control.
▪ When inclining the table top and the 0°
position has been reached.
▪ When tilting the table top and the 0° posi-
tion has been reached.
▪ When reaching the CENTRAL position
during table top adjustment.
This signal tone can, with the exception of
the warnings, be deactivated / activated in
the [Settings, Signal tone of the column]
menu.
Continuous tone
The continuous tone will sound once the end
position of the adjustment function has been
reached as long as this button is pressed on
the hand control.
This signal tone can, with the exception of
the warnings, be deactivated / activated in
the [Settings, Signal tone of the column]
menu.
Slow intermittent tone (2 signal tones per
second)
The slow intermittent tone will sound in the
following cases:
▪ An operating function is being executed
and a warning is shown on the display of
the hand control.
This signal tone can be deactivated / activ-
ated in the [Settings, Signal tone of the OR
table] menu in some cases.
Quick intermittent tone (4 signal tones
per second)
The quick intermittent tone is sounded in the
following cases:
▪ The rechargeable battery of the OR table
is fully discharged.
Tab. 7: Acoustic signals issued by the OR table
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IFU 7200.01 EN 11 71 / 150
Operation and use
5 OR table
5.2.2 Setting up equipotential bonding
WARN IN G !
Risk of injury!
Without equipotential bonding, products with differing electrical potentials
may cause short circuits on the operating table.
Establish potential bonding prior to each use of the operating table.
NO TE
The electrical conductivity of the product has to be checked annually by an author-
ised service technician.
1. Connect the supplied equipotential bond-

ing cable to the equipotential bonding pin
1 on the mobile operating table.
2. Connect the other end of the equipotential

bonding cable to the operating room's
equipotential bonding pin.
Fig. 50: Setting up equipotential bonding
5.2.3 Status indicators mains connection / battery charge state

The status display is located on the override control panel [8 Page 40].
5.2.3.1 Overview of status display for mains connection
Symbol Meaning LED Condition Status

colour
Network connec- Green Continu- Mains operation
tion ous light (The mains cable is connected to the OR
table and the power supply network.)
- Off Battery operation
(The mains cable is not connected to the
OR table.
The mains cable is not connected to the
power supply network.)
Tab. 8: Overview of status indicator for mains connection
7200.01XX
72 / 150 IFU 7200.01 EN 11
Operation and use
OR table 5
5.2.3.2 Overview of status display for battery charge state

colour
Battery charge Green Continu- In mains operation: Battery fully recharged
level ous light
Flashing In mains operation: Battery is being
light charged, charging capacity sufficient for bat-
tery operation
Fast flash- In rechargeable battery operation: Charging
ing light capacity sufficient for battery operation
Orange Flashing In mains operation: Battery charged, char-
light ging capacity insufficient for battery opera-
tion
if battery capacity is very low, a signal will
sound as a light flashes and the adjustment
speed of the OR table will be reduced
Fast flash- In rechargeable battery operation: Charging
ing light capacity insufficient for continued battery
operation, battery must be charged
if battery capacity is very low, a signal will
sound as a light flashes, a warning notice
will be displayed on the control device, and
the adjustment speed of the OR table will be
reduced
Red Flashing In mains operation: Battery defective
light a signal will sound as a light flashes and the
adjustment speed of the OR table will be re-
duced
Fast flash- In rechargeable battery operation: Battery
ing light fully discharged and not ready for operation,
battery must be charged immediately or is
defective
a signal will sound as a light flashes, a
warning notice will be displayed on the con-
trol device, and the OR table cannot be ad-
justed
- Off In mains operation: Battery defective
a signal will sound and the adjustment
speed of the OR table will be reduced
In rechargeable battery operation: OR table
in stand-by mode. Rechargeable battery
must be charged, or is defective
Tab. 9: Overview of status display for battery charge state
7200.01XX
IFU 7200.01 EN 11 73 / 150
Operation and use
5 OR table
5.2.4 Battery operation
NO TE
When running on battery power, without the mains cable being connected, the mo-
bile operating is approved for use in Class AP-M hazardous locations.
Please note:
• A complete charging cycle takes about 12 hours.
• The mobile OR table switches off automatically if the charging capacity is less than 15%.
• If the battery charge level is too low, this is indicated on the display of the control unit and the
status indicator of the override control panel.
• As soon as the operating table is connected to the mains network via the mains cable, the
batteries are automatically charged.
5.2.5 Deep discharge protection

The deep discharge protection is a function of the OR table designed to protect the battery. When
the deep discharge protection function is activated, the supply of electronic components is dis-
connect from the battery. The operating table can no longer be controlled using the hand con-
trols. The batteries are reactivated by connecting the mains voltage.
5.2.5.1 Automatic deep discharge

If the OR table is not supplied with mains voltage for 7 days, the deep discharge protection func-
tion is activated automatically.
5.2.5.2 Activate deep discharge protection manually
1. Press the button combination [Blue up] 1 ,

[Blue down] 2 and [0-position] 3 and
1
hold for at least 3 seconds.
Ø During the first 3 seconds a signal tone
2 will be sounded periodically.
Ø A single acoustic signal will sound after
3 seconds to indicate that deep dis-
charge protection has been activated.
2. Release the button combination.
3 Ø Deep discharge protection is activated.
Fig. 51: Activate deep discharge protection

manually
7200.01XX
74 / 150 IFU 7200.01 EN 11
Operation and use
OR table 5
5.2.6 Charge batteries (mains operation)
DA NG ER !
Risk of explosion!
When connected to the power supply the OR table is not authorised for use
in explosion prone AP-M areas.
An explosion could occur when using disinfectants or cleaning agents con-
taining alcohol, or flammable anaesthetics which are blended with air, oxy-
gen or nitrous oxide.
When operating on the mains supply, never use disinfectants, cleaning agents con-
taining alcohol, or flammable anaesthetics which are blended with air, oxygen or ni-
trous oxide!
DA NG ER !
Potentially fatal due to electrical shock!
Only connect product to voltage supply with protective earth connection.
WARN ING !
The product can no longer be adjusted if the batteries are discharged and the
mains supply is interrupted.
Connect the product for mains operation to an uninterrupted power supply (UPS)
or to a stationary emergency power generator.
NO TE
In order to prevent the charging of the battery during OR operation, it is recommen-
ded to charge the rechargeable battery after OR use and on a daily basis. On prin-
ciple, deep discharge of the rechargeable battery should be avoided.
NO TE
The OR table is disconnected from the mains by means of the plug.
Connecting to mains supply

1. Make sure that there are no liquid residues
on the power supply of the OR table.
2. If necessary, remove any liquid residues.
3. Connect the supplied mains cable 1 to
the mains connection 2 of the OR table.
1
4. Plug into the mains power outlet.
Ø The status display for mains operation
on the override control panel is illumin-
ated green.
2
Ø The rechargeable batteries of the OR
table are charged.
Ø The plug must always be accessible to
ensure that the OR table can be discon-
nected from the power supply at any
time.
Fig. 52: Establishing / separating the mains con-
nection Detach the mains cable
1. Detach the plug at the main socket.
2. Detach the mains cable from the operating
table.
7200.01XX
IFU 7200.01 EN 11 75 / 150
Operation and use
5 OR table
5.2.7 Displacing / locking the OR table
WARN IN G !
Risk of tipping over!
The OR table can tip over while extending the OR table swivel castors if the
maximum height is exceeded.
Before extending the OR table swivel castors [UNLOCK], ensure that the protru-
sion and the 850 mm maximum height of the OR table are complied with. The
height of the OR table is lower than 850 mm if the red area of the adhesive label on
the column is no longer visible.
WARN IN G !
WARN IN G !
Risk of injury!
Hold the OR table firmly before extending the swivel castors [UNLOCK] in order to
ensure that the OR table cannot roll away unintentionally.
CA UTIO N !
Property damages caused as a result of collision when moving/adjusting the
mobile operating table!
Remove potential hindrances before moving / adjusting the mobile operating table
and avoid collisions.
CA UTIO N !
Property damage!
When moving the OR table use at least one hand in order to prevent any collisions.
7200.01XX
76 / 150 IFU 7200.01 EN 11
Operation and use
OR table 5
5.2.7.1 Status display [LOCK] / [UNLOCK]

The status display is located on the override control panel [8 Page 40].

colour
LOCK Green Flashing OR table switches status LOCK / UN-
light (altern- LOCK.
ates with
UNLOCK)
Continuous OR table is locked
light
UNLOCK Orange Flashing OR table switches status LOCK / UN-
light (altern- LOCK.
ates with
LOCK)
Continuous OR table is on castors.
light
Tab. 10: Status display LOCK / UNLOCK
5.2.7.2 Moving the OR table without autodrive [UNLOCK]
CA UTI ON !
Property damage!
When moving the mobile operating table, there is a risk of collision with the
environment.
In order to avoid collisions when moving the mobile operating table, two people
should guide the OR table.
1. Unplug the mains cable and equipotential bonding cable from the OR table.
2. Press the [UNLOCK] button for at least 1 second.
Ø The Lock Menu menu will open on the control device.

Ø The swivel castors extend automatically.
Ø LED below the [UNLOCK] button on the override control panel lights up.
Ø OR table can be moved.
3. Use two people to guide the OR table.
7200.01XX
IFU 7200.01 EN 11 77 / 150
Operation and use
5 OR table
5.2.7.3 Moving the OR table using autodrive [UNLOCK]
NO TE
The operating table can be moved in both longitudinal and transverse directions.
The swivel castors set themselves to the direction of the most recent motion. If the
OR table is to be moved at an angle of 90° to the most recent direction of motion,
increased exertion of force is required, since the swivel castors are positioned
across the desired direction of travel. If the swivel castors are positioned across the
required direction of travel, it is easier to move the OR table if you start off diagon-
ally to the required direction of travel (angle of approximately 45°).
The assistance of a second person might be required here.
Extend the swivel castors (UNLOCK)

Prerequisites:
3 2
• Mains cable and equipotential bonding
cable are unplugged from the OR table.
1. Push and hold the [UNLOCK] 1 button.
Ø The swivel castors extend automatic-
ally.
Ø The DRIVE menu will open on the con-
trol device.
Ø LED below the [UNLOCK] button on the
override control panel lights up.
1
Ø Hold the OR table with at least one
Fig. 53: Moving the operating table using the hand.
motor
- or -
OR01-14
1. Press the [UNLOCK] 1 button for 1
BACK second.
DRIVE Ø The DRIVE menu will open on the con-

trol device.
Backward Forward 2. Press [Multifunction button down].
Ø The swivel castors extend automatic-
ally.
Ø Hold the OR table with at least one
hand.
Moving the OR table

Backward Unlock
1. Press [Multifunction button right] 2 or
Lock Forward
[Multifunction button left] 3 .
Fig. 54: DRIVE operating menu Ø The OR table moves in the appropriate
direction at speed.
7200.01XX
78 / 150 IFU 7200.01 EN 11
Operation and use
OR table 5
2. Press [Multifunction button right] 2 or

[Multifunction button left] 3 2× and hold.
Ø The OR table moves in the appropriate
direction at increased speed.
3. Guide the OR table with at least one hand.
4. Release [Multifunction button right] 2 or
[Multifunction button left] 3 at the desired
position.
Ø The OR table stops moving.
5.2.7.4 Locking the OR table [LOCK]
NO TE
Carry out the adjustment functions of the OR table only with the swivel castors re-
tracted (LOCK).
If an adjustment function is performed without retracting the swivel castors (UN-
LOCK), a message appears on the display of the control device indicating that the
swivel castors must be retracted.
CANCEL OK • The Lock Menu menu is open.
LOCK MENU 1. Push and hold the [Multifunction button
down].
Operating Table Lock
Ø The swivel castors retract automatic-
Table Top Lock
ally.
Wheel Lock disabled Ø LED below the [LOCK] button on the
override control panel lights up.
Ø OR table is locked.
Ø The OR table can be adjusted.
Unlock
Lock
Fig. 55: Locking the OR table [LOCK]
7200.01XX
IFU 7200.01 EN 11 79 / 150
Operation and use
5 Table tops and accessories
5.3 Table tops and accessories
5.3.1 Mounting the table width extensions (1001.75A0 / 76A0)
WARN IN G !
The following accessories may be mounted to the table width extensions
(1001.75A0) and (1001.76A0):
• 1x anaesthesia screen (1002.57A0)
• 1x arm restraint cuff (1002.24C0)
• 1 x arm protector (1002.25A0)
The patient must lie above the centre of the column.
WARN IN G !
No additional table width extenders may be mounted to the table width extenders
(1001.75A0) and (1001.76A0).
Mounting the table width extension

1. Attach the locking clamp 1 of the table
width extension to the side rail 2 .
2. Tighten the drop toggle screw 3 .
3. Check firm seat of the table width exten-
sion.
1
3
2
Fig. 56: Mounting the table width extension
7200.01XX
80 / 150 IFU 7200.01 EN 11
Operation and use
Table tops and accessories 5
5.3.2 Mounting / removing the head rest
NO TE
Use and handling are described in detail in the product-specific instructions for use.
NO TE
In order to mount head rests to the NORMAL / REVERSE mounting points, the
head rest adapter (1130.81A0) is required.
Head rests may be mounted via the extension plate (1131.31BC/FC) or in conjunction with the
head rest adapter (1130.81A0), directly to the NORMAL / REVERSE mounting points.
5.3.2.1 Mounting and removing the head rest using the head rest adapter (1130.81A0)
NO TE
The head rest adapter consists of a left and a right part. If the adapters are mixed
up, the distance of the drilled holes will correspond: Observe the markings L and R.
Mounting the head rest

1
1. Insert the pins of the head rest adapter 1
fully into the front end mounting points 2
1 on both sides of the table top.
Fig. 57: Mount the head rest adapter
2. Insert the pins of the head rest 3 fully into

3
the front end mounting points 4 of the
table top.
Fig. 58: Mounting the head rest
7200.01XX
IFU 7200.01 EN 11 81 / 150
Operation and use
3. Tighten the drop-toggle set screw 5 .

4. Check the secure seating of the head rest
by pulling on it on both sides.
Fig. 59: Secure the head rest
Remove the head rest

3
1. Loosen the drop toggle screw 5 .
1
2. Remove the head rest 3 .
3. Remove the two head rest adapters 1 .
Fig. 60: Removing the head rest
7200.01XX
82 / 150 IFU 7200.01 EN 11
Operation and use
5.3.3 Extension plate (1131.31BC)
NO TE
Adjustment of the REVERSE mounting point (leg plate mounting point) may result
in a slight misalignment of the two table top supporting arms after some time.
At regular intervals align the leg plates or the one-section accessory using the
[LEVEL] button and the [Leg plate up] button to correct any offset. [8 Page 47]
The table top can be extended to enable the positioning of taller patients or to optimise the pa-
tient position. Extension can be mounted on both the NORMAL / REVERSE mounting points of
the table top.
Mounting the extension plate

1
1. If necessary, remove the head rest
[8 Page 81].
2. Insert the pins of the extension plate 1
fully into the front end mounting points 2 .
Ø The extension plate is locked automat-
ically.
3. Check that the extension plate is firmly po-
2
sitioned.
Fig. 61: Mounting the extension plate
Removing the extension plate

2
1. Press both release levers 1 against the
extension plate.
2. Pull the extension plate 2 out of the front
end mounting points without tilting.
1
1
Fig. 62: Removing the extension plate
7200.01XX
IFU 7200.01 EN 11 83 / 150
Operation and use
5.3.4 Mounting and removing the seat plate extension (1131.55BC )
NO TE
The table top can be extended with a seat plate extension to enable the positioning of taller pa-
tients or to optimise the patient position. Seat plate extension can be mounted on both the NOR-
MAL / REVERSE mounting points of the table top.
Mounting the seat plate extension

1
1. If necessary, remove the leg plate or
transfer board.
2. Insert the pins 1 of the seat plate exten-
sion fully into the front end mounting point
2 of the table top.
Ø The seat plate extension is locked auto-

matically.
2 3. Check the firm seat of the seat plate ex-
2
tension.
Fig. 63: Mounting the seat plate extension
Removing the seat plate extension

1
1. If necessary, remove the leg plate or
transfer board.
2. Press both release levers 3 against the
seat plate extension.
3. Pull the seat plate extension 1 out of the
front end mounting points without tilting it.
Fig. 64: Removing the seat plate extension
7200.01XX
84 / 150 IFU 7200.01 EN 11
Operation and use
5.3.5 Mounting / removing the leg plates
NO TE
Leg plates can be mounted on both the NORMAL / REVERSE mounting points of the table top.
5.3.5.1 Mounting / removing the pair of leg plates (1133.53BC)
Mounting the pair of leg plates

2
1. Push the release button 1 down and
hold.
2. Insert the leg plates 2 fully into the
mounting point 3 .
3 Ø The side rail of the leg plate is facing to-

wards the outside.
3. Release the release button.
Ø The leg plate is locked automatically.
4. Check the firm seat of the leg plate.
5. Mount the second leg plate in the same
1
way as the first leg plate.
Fig. 65: Mounting the pair of leg plates
Removing the pair of leg plates

1. Push the release button 1 down and
hold.
2. Pull the leg plate 2 out of the mounting
point without tilting.
2 3. Release the release button.
4. Remove the second leg plate in the same
way as for the first leg plate.
Fig. 66: Removing the pair of leg plates
7200.01XX
IFU 7200.01 EN 11 85 / 150
Operation and use
5.3.5.2 Mounting / removing the leg plate (1133.58BC)
Mounting the leg plate

1. Pull the release lever 1 .
2 2. Slide the pins 2 of the leg plate as far as
they will go into the mounting point 3 .
Ø The safety catch engages automatic-
ally.
3. Let go of the release lever.
Ø Leg plate is locked.
3
4. Check the firm seat of the leg plate.
Fig. 67: Mounting the leg plate
Removing the leg plate

2
1. Pull the release lever 1 .
2. Pull the leg plate 2 out of the mounting
point.
3. Let go of the release lever.
Fig. 68: Removing the leg plate
7200.01XX
86 / 150 IFU 7200.01 EN 11
Operation and use
5.3.6 Attaching the X-ray top (1131.80A0), optional

After mounting the X-ray top, X-ray cassettes may be inserted on the side below the X-ray top.
WARN ING !
The overall load of may not exceed 250 kg.
WARN ING !
Risk of injury for personnel caused by squeezing and shearing!
Risk of injury caused by squeezing and shearing when mounting the indi-
vidual plates of the X-ray top.
Mount the plates of the X-ray top with special care.
NO TE
When the X-ray top is attached, the lowest operating table position will be raised by
approximately 50 mm (2 inches).
NO TE
To insert X-ray cassettes, align the OR table horizontally.
5 6
2 4
1 3
Fig. 69: Overview of X-ray top
1 X-ray top for head rest (1130.64C0) 4 X-ray top for seat plate
2 X-ray top for extension plate (1131.31BC/FC) 5 X-ray top for seat plate extension (1131.55BC/
3 X-ray top for back plate FC)
6 X-ray top for leg plate (1133.58BC/FC)
7200.01XX
IFU 7200.01 EN 11 87 / 150
Operation and use
5.3.6.1 Mounting / removing the X-ray top
CA UTIO N !
Property damage!
The X-ray top may fall as a result of the adjustment of the leg or back plate.
With the X-ray top, the table top must always be aligned horizontally.
Always remove the X-ray top before adjusting the leg or back plate.
Prerequisites:
• Two circlips made from rubber are at-
tached to each segment of the x-ray top.
• The circlips are located on two diagonally
positioned pins on each segment.
Mounting the x-ray top

1. Remove the pad.
2. Insert the pins 1 of the x-ray top seg-
1 ments into the holes drilled in the table top
2.
3. Check the firm seating of the segments.

2 4. Mount the pad.
5. Check the firm seat of the pad.
Removing the X-ray top

Fig. 70: Mounting the x-ray top
1. Remove the padding.
2. Remove the X-ray top segment by pulling
upwards gently.
3. Install the padding.
4. Check the firm seat of the padding.
7200.01XX
88 / 150 IFU 7200.01 EN 11
Operation and use
5.3.7 Removing / mounting pads
Removing the pad

1. Grasp and remove the pad (1) with both
hands.
Fig. 71: Removing the pad
Attaching the pad

1. Position the pad in such a way that the
hook and loop tapes line up.
2. Firmly push down on the pad.
Ø Pad cannot be moved.
3. Check proper fit.
Fig. 72: Attaching the padding
7200.01XX
IFU 7200.01 EN 11 89 / 150
Operation and use
5 Explanation of instructions for use
5.4 Explanation of instructions for use

Labels providing instructions for use are affixed to the product. Their meaning is explained below.
5.4.1 CENTRAL position
Fig. 73: Notes for use: CENTRAL position
The CENTRAL position instruction for operation is located at column height on the OR table
base.
With an overall load of 250 kg, the OR table may only be used if the OR table is in the CENTRAL
position: The longitudinal shift of the OR table is lifted and the centre table top bar 1 is above
the column 2 .
5.4.2 Maximum height when moving the OR table with an overall load of up to
250 kg
With an overall load of up to 250 kg, the lock

of the OR table may only be released if the
OR table is set to a maximum height of
850 mm (lower edge of pad). If the red section
of the label on the column casing is visible, the
maximum height of 850 mm of the OR table
has been exceeded. In this case, reduce the
height of the OR table before moving it
Fig. 74: Height for operating table lock
7200.01XX
90 / 150 IFU 7200.01 EN 11
Approved accessories and table top configuration
6
6 Approved accessories and table top configuration
DA NG ER !
Potentially fatal!
Patient may be endangered as a result of incorrect use.
Follow the instructions for use for all accessories.
DA NG ER !
REVERSE patient orientation is not permitted with an overall load exceeding
250 kg.
WARN ING !
Risk of injury due to overloading!
The permitted load of the product depends on the combination of accessor-
ies used.
The product with the lowest permissible load determines the maximum load in the
event that it is combined with other accessories.
Refer to the instructions for use of each accessory for the permissible load.
WARN ING !
Risk of injury due to tipping over of the OR table!
Depending on the overall load, the OR table may only be used with restric-
tions.
Always observe all usage-related restrictions that result in accordance with the
overall load of the OR table.
WARN ING !
Risk of tipping over!
The OR table can tip over while extending the OR table swivel castors if the
maximum height is exceeded.
Before extending the OR table swivel castors [UNLOCK], ensure that the protru-
sion and the 850 mm maximum height of the OR table are complied with. The
height of the OR table is lower than 850 mm if the red area of the adhesive label on
the column is no longer visible.
7200.01XX
IFU 7200.01 EN 11 91 / 150
6
WARN IN G !
NO TE
Patients should preferably be positioned in NORMAL patient orientation on the
table top.
The images in this chapter show the accessories that can be used to configure the OR table
within the respective overall load range.
7200.01XX
92 / 150 IFU 7200.01 EN 11
Table top configuration for an overall load up to 155 kg 6
6.1 Table top configuration for an overall load up to 155 kg
6.1.1 NORMAL patient orientation / OR table can be moved (UNLOCK)
1002.15XX
1133.53XX
1002.71XX 1132.34XX
1160.50XX
1007.16XX
1002.72XX
1130.70XX
1002.82XX
1002.73XX
1433.33XX 1132.65XX
1005.49XX
1160.55XX
1002.73XX
1002.07XX
1002.72XX 1133.53XX
1160.35XX 1160.32XX
1002.71XX
1133.58XX
1007.16XX 1131.55XX
1160.32XX
1160.53XX
1133.67XX
1002.07XX
1130.54XX
1005.50XX 1160.64XX
1160.55XX
1005.58XX 1133.73XX
1
1130.53XX
1130.81XX
1130.64XX
155 kg /
1130.67XX 340 lb
1130.69XX
7200.01
1002.74XX
Fig. 75: Table top configuration 1 of 2 for an overall load of up to 155 kg, NORMAL patient orientation,
OR table can be moved [UNLOCK]
7200.01XX
IFU 7200.01 EN 11 93 / 150
6 Table top configuration for an overall load up to 155 kg
1160.53XX
1002.07XX 1160.64XX
1130.54XX
1005.50XX 1 1160.55XX
1005.58XX
1130.53XX
1130.81XX 1160.32XX
1130.64XX
1131.55XX
1131.31XX
1130.67XX
1130.81XX
1130.69XX
1130.81XX
1002.74XX
155 kg /
340 lb
7200.01
7200.01XX
94 / 150 IFU 7200.01 EN 11
6.1.2 REVERSE patient orientation/ OR table can be moved (UNLOCK)
1002.07XX 1002.73XX
1002.72XX
1160.35XX
1130.56XX
1007.16XX 1002.71XX
1160.55XX
1160.50XX
1160.53XX
e
L
or
1130.70XX 1160.64XX
1160.32XX
1
1160.55XX
1132.65XX
1002.82XX
1133.53XX 1160.32XX 1433.33XX 1005.49XX
1133.58XX 1005.48XX
1131.55XX 1433.34XX
1133.67XX
1002.10XX
1133.73XX
155 kg /
340 lb
7200.01
Fig. 77: Table top configuration 1 of 2 for an overall load of up to 155 kg, REVERSE patient orientation,
7200.01XX
IFU 7200.01 EN 11 95 / 150
1002.15XX
1007.18XX
1007.16XX
1002.71XX
1007.21XX
1002.72XX
1132.34XX
1007.16XX 1002.73XX
1002.73XX
1160.35XX
1002.07XX
1002.72XX
1160.55XX 1160.53XX
1002.71XX
1131.55XX
1007.16XX
1160.64XX
1160.32XX 1130.53XX
1
1130.81XX
1130.64XX
1131.31XX
1130.81XX 1130.67XX
1130.81XX
1130.69XX
1002.74XX
155 kg /
340 lb
7200.01
7200.01XX
96 / 150 IFU 7200.01 EN 11
6.1.3 NORMAL patient orientation/OR table locked (LOCK)
1007.04XX
1002.07XX
1130.54XX
1005.50XX 1160.55XX
1419.01XX
1005.58XX 1003.37XX
1130.53XX
1160.32XX
1130.64XX
1131.55XX
1131.31XX
1130.67XX 1130.56XX
1130.70XX
1130.69XX 1130.81XX
1132.65XX
1130.81XX
1002.74XX
1133.53XX
1131.55XX
1133.58XX
1002.15XX 1160.55XX
1133.67XX
1132.34XX 1160.32XX
1007.16XX
1002.71XX 1133.73XX
1002.72XX
1160.50XX
1002.73XX
155 kg /
340 lb
7200.01
OR table is locked [LOCK]
7200.01XX
IFU 7200.01 EN 11 97 / 150
1002.82XX
1433.33XX
1005.49XX
1005.48XX
1002.73XX
1002.07XX
1002.72XX
1160.35XX
1002.71XX
1002.07XX 1007.16XX
1005.50XX 1130.54XX
1005.58XX
1160.55XX
1130.53XX
1160.53XX
1130.64XX 1160.32XX
1160.64XX
1130.67XX 1
1130.69XX
1130.81XX
1002.74XX
155 kg /
340 lb
7200.01
7200.01XX
98 / 150 IFU 7200.01 EN 11
6.1.4 REVERSE patient orientation/OR table locked (LOCK)
1002.82XX
1433.33XX 1005.49XX
1433.34XX 1005.48XX
1002.10XX
1130.70XX
1002.73XX
1002.07XX
1002.72XX
1132.65XX
1160.55XX
1160.35XX 1002.71XX
1133.53XX
1160.32XX 1007.16XX
1133.58XX 1160.53XX 1130.53XX
1131.55XX
1160.55XX
1133.67XX 1160.64XX 1130.64XX
1160.64AC
1133.73XX 1130.67XX
1130.81XX
1160.32XX 1130.69XX
1160.50XX
1002.74XX
155 kg /
340 lb
7200.01
7200.01XX
IFU 7200.01 EN 11 99 / 150
1002.15XX
1132.45XX
1131.55XX 1132.34XX
1002.71XX
1007.16XX
1002.72XX
1131.31XX
1002.07XX
1160.55XX 1130.54XX
1005.50XX 1002.73XX
1160.55XX
1005.58XX
1130.53XX
1160.32XX 1160.32XX
1130.81XX
1130.64XX
1130.81XX
1130.67XX
1419.01XX 1130.69XX
1003.37XX
1002.74XX
1130.56XX 1007.24XX
155 kg /
340 lb
7200.01
7200.01XX
100 / 150 IFU 7200.01 EN 11
Table top configuration with an overall load of 155-250 kg 6
6.2 Table top configuration with an overall load of 155-250 kg
6.2.1 NORMAL patient orientation / OR table can be moved (UNLOCK)
1002.73XX
1002.07XX
1002.72XX
1160.35XX 1160.55XX
1133.53XX
1002.71XX
1007.16XX 1160.32XX
1133.58XX
1131.55XX
1002.82XX
1433.33XX 1133.58XX
1005.49XX
1005.48XX
1160.50XX
1002.15XX
1132.34XX 1133.67XX
1002.71XX 1007.16XX
1133.73XX
1002.72XX
1002.73XX
250 kg /
555 lb
7200.01
Fig. 83: Table top configuration 1 of 2 for an overall load of 155-250 kg, NORMAL patient orientation,
7200.01XX
IFU 7200.01 EN 11 101 / 150
6 Table top configuration with an overall load of 155-250 kg
1002.73XX
1002.07XX 1160.35XX
1160.55XX
1002.72XX 1160.53XX
1160.32XX
1160.64XX
1
1002.71XX
1160.35XX
1007.16XX
1160.53XX
1160.55XX 1131.55XX
1160.64XX
1002.07XX
1160.32X
1130.54XX
1005.50XX
1005.58XX
1130.81XX
1130.53XX
1131.31XX
1130.64XX
1130.81XX
1130.67XX
1130.81XX
1130.69XX
250 kg /
555 lb
1002.74XX
7200.01
7200.01XX
102 / 150 IFU 7200.01 EN 11
6.2.2 REVERSE patient orientation / OR table can be moved (UNLOCK)
1131.55XX 1131.31XX
1130.54XX
1002.07XX
1005.50XX
1130.81XX
1005.58XX
1130.81XX
1160.55XX 1130.53XX
1002.82XX
1133.53XX
1160.32XX 1433.33XX 1130.64XX

1005.49XX
1133.58XX
1433.34XX 1130.67XX
1005.48XX
1131.55XX
1002.10A0
1130.69XX
1133.58XX
1130.81XX
1160.55XX
1002.74XX
1160.53XX
1160.50XX
1160.64XX 1002.73XX
1160.32XX
1160.64AC 1002.07XX
1133.67XX 1002.72XX
1160.35XX
1002.71XX
1133.73XX
1007.16XX
250 kg /
555 lb
7200.01
Fig. 85: Table top configuration for an overall load of 155–250 kg, REVERSE patient orientation, UN-
LOCK
7200.01XX
IFU 7200.01 EN 11 103 / 150
1002.82XX
1433.33XX
1005.49XX
1160.55XX
1005.48XX 1133.53XX
1160.32XX
1002.07XX
1130.54XX
1005.50XX 1133.58XX
1130.81XX
1005.58XX
1131.55XX
1130.53XX
1160.55XX
1133.64XX
1133.58XX
1130.81XX 1160.32XX
1130.67XX
1160.50X
1130.69XX
1133.67XX
1002.74XX
1002.15XX 1133.73XX
1132.34XX
1007.16XX
1002.71XX
250 kg /
555 lb
1002.72XX
1002.73XX
7200.01
7200.01XX
104 / 150 IFU 7200.01 EN 11
1002.73XX
1002.07XX 1160.35XX
1160.55XX
1002.72XX 1160.53XX
1160.32XX
1160.64XX
1
1002.71XX
1160.35XX
1007.16XX
1160.53XX
1160.55XX 1131.55XX
1160.64XX
1002.07XX
1160.32X
1130.54XX
1005.50XX
1005.58XX
1130.81XX
1130.53XX
1131.31XX
1130.64XX
1130.81XX
1130.67XX
1130.81XX
1130.69XX
250 kg /
555 lb
1002.74XX
7200.01
7200.01XX
IFU 7200.01 EN 11 105 / 150
6.2.4 REVERSE patient orientation/OR table locked (LOCK)
1007.24XX
1002.73XX
1002.07XX
1002.72XX
1002.71XX
1160.35XX
1007.16XX
1160.53XX
1160.55XX
1160.64XX
1160.64AC
1130.54XX
1160.32XX 1002.07XX
1130.81XX
1005.50XX
1131.55XX
1005.58XX
1131.31XX
1130.53XX
1130.81XX 1130.64XX
1130.81XX 1130.67XX
1130.69XX
250 kg /
1130.74XX
555 lb
7200.01
Fig. 88: Table top configuration 1 of 2 for an overall load of 155-250 kg, REVERSE patient orientation,
7200.01XX
106 / 150 IFU 7200.01 EN 11
1130.54XX
1002.07XX
1005.50XX
1002.82XX
1160.55XX
1005.58XX
1133.53XX 1433.33XX 1130.53XX

1005.49XX
1160.32XX
1130.64XX
1133.58XX 1433.34XX 1005.48XX
1131.55XX
1002.10XX 1130.67XX
1130.69XX
1133.58XX
1130.81XX
1160.55XX
1002.74XX
1160.53XX
1160.50XX
1160.64XX 1002.73XX
1160.32XX
1160.64AC 1002.07XX
1133.67XX 1002.72XX
1160.35XX
1002.71XX
1133.73XX
1007.16XX
250 kg /
555 lb
7200.01
Fig. 89: Table top configuration 2 of 2 for an overall load of 155-250 kg, REVERSE patient orientation,
7200.01XX
IFU 7200.01 EN 11 107 / 150
6 Table top configuration with an overall load of 250–450 kg
6.3 Table top configuration with an overall load of 250–450 kg
6.3.1 Usage-related restrictions for 250-454 kg

• Longitudinal shift not permitted. The OR table may only be used in the CENTRAL position.
• Maximum permitted inclination: ±20°
• Maximum permitted lateral tilt: ±5°
• Maximum permitted back plate adjustment: +70° / -10°
• BEACH CHAIR position for adiposity surgery only permitted if the required supports are taken
into account.
• Only use accessories that are permitted for the OR table in accordance with the overall load
of the OR table.
7200.01XX
108 / 150 IFU 7200.01 EN 11
Table top configuration with an overall load of 250–450 kg 6
1160.55XX
1160.64XX
CA46.0611
1160.32XX
1133.53XX
1131.31XX
1130.64XX 1133.58XX
1130.67XX
1130.81XX
454 kg /
1000 lb
7200.01
Fig. 90: Table top configuration for an overall load of 250-454 kg, NORMAL patient orientation, LOCK
7200.01XX
IFU 7200.01 EN 11 109 / 150
6 Approved accessories
6.4 Approved accessories

The following tables list the accessory variations permitted for use with the table top or OR table.
6.4.1 Side rail accessories

Only Maquet side rail accessories are authorised for use on the side rails. The maximum load of
the side rails is 20 kg.
Accessories made by other manufacturers may only be used with permission from Maquet.
6.4.2 Hand controls

1009.81J0 Foot switch
7200.90A0 Corded hand control
7200.91A0 IR remote control
Tab. 11: Hand controls
6.4.3 Maximum overall load up to 155 kg
6.4.3.1 Accessories for NORMAL mounting point up to 155 kg
1001.40A0 Arm protector

1002.07A0 Head rest adapter
1002.15A0 Head support for shoulder operations
1002.71A0 Horseshoe head rest
1002.73A0 Head rest
1002.74A0/B0 Motorised head rest adjustment
1002.82A0 Rigid head rest
1003.44A0 Soiled instrument bowl
1003.45D0 TUR rinsing set
1005.01B0 Knee crutches
1005.03A0 Calf crutches
1005.49A0 Skull clamp by Integra
1005.49B0 Skull clamp from Promed
1005.50A0 Standard holder
1005.5800 Support arm
1005.78C0 Paediatric OR table top
1007.53A0 Kneeling frame
1118.50B0/F0 Pair of leg plates
1130.53B0 Head rest
1130.54B0 Connection bracket
1130.56A0 Rectal positioning device
1130.64C0 Head rest
Tab. 12: Accessories for NORMAL mounting point up to 155 kg
7200.01XX
110 / 150 IFU 7200.01 EN 11
Approved accessories 6
1130.64G0 Head rest

1130.65A0/B0 Transfer board
1130.67B0/F0 Head rest with gas-strut assisted adjustment
1130.69B0/F0 Dual-joint head rest
1130.70AC MAQUETMATIC
1131.31BC/FC Extension plate
1131.55BC/FC Seat plate extension
1132.34A0 Back plate for shoulder surgery
1132.45AC Carbon fibre back plate
1132.65A0 Transfer board
1133.53BC/FC Pair of leg plates
1133.58BC/FC Leg plate, one-piece
1133.67BC Pair of leg plates
1150.70A0 Accessory adapter
1150.72A0/F0 Accessory adapter
1160.32AC/BC/DC/ Extension plate
FC/GC
1160.35AC/BC Trapezoidal back plate
1160.50AC/BC/DC/ Pair of leg plates
FC/GC
1160.53AC/BC/FC/ Dual-joint head rest
GC
1160.55AC/BC/DC/ Seat plate extension
FC/GC
1160.64AC/BC/FC/ Head rest
GC
1419.04A0 Pair of adapters
1419.04G0 Pair of adapters
1419.05A0 Pads with pelvis plate
1419.05B0 Pads with pelvis plate
Tab. 12: Accessories for NORMAL mounting point up to 155 kg
6.4.3.2 Accessories for the NORMAL mounting point up to 155 kg, OR table locked (LOCK)
When the OR table is locked (LOCK), the following accessories can also be mounted to the OR
table.
1003.3700 Screw tension device

1419.01A0 Extension device
1419.01B0 Extension device
1419.01JC Extension device
Tab. 13: Accessories for the NORMAL mounting point up to 155 kg, OR table locked (LOCK)
7200.01XX
IFU 7200.01 EN 11 111 / 150
6.4.3.3 Accessories for REVERSE mounting point up to 155 kg
1001.40A0 Arm protector

1002.10A0 Adjustable head rest adapter
1002.73A0 Head rest
1002.74A0 Motorised head rest adjustment
1003.44A0 Soiled instrument bowl
1003.45D0 TUR rinsing set
1003.66A0/B0 Traction set
1005.01B0 Knee crutches
1005.03A0 Calf crutches
1005.48A0/B0 Skull clamp holder
1005.78C0 Paediatric OR table top
1007.16A0/B0 Head rest adapter
1007.18B0/F0 Back plate for shoulder operations
1007.21B0/F0 Back plate for shoulder surgery
1007.53A0 Kneeling frame
1118.50B0/F0 Pair of leg plates
1130.53B0 Head rest
1130.64C0 Head rest
1130.64G0 Head rest
1130.65A0/B0 Transfer board
1150.72A0/F0 Accessory adapter
Tab. 14: Accessories for REVERSE mounting point up to 155 kg
7200.01XX
112 / 150 IFU 7200.01 EN 11
1419.04G0 Pair of adapters

1419.05B0 Pads with pelvis plate
1433.34AC/FC Carbon fibre back plate for shoulder surgery
FC/GC
FC/GC
GC
FC/GC
GC
Tab. 14: Accessories for REVERSE mounting point up to 155 kg
6.4.3.4 Accessories for the REVERSE mounting point up to 155 kg, OR table locked (LOCK)
table.
1003.3700 Screw tension device

1007.04BC Kneeling frame, coded
1007.24A1/F1 Universal frame for positioning patients
1130.56A0 Rectal positioning device
1419.01JC Extension device
Tab. 15: Accessories for the REVERSE mounting point up to 155 kg, OR table locked (LOCK)
6.4.4 Maximum overall load 155–250 kg
6.4.4.1 Accessories for NORMAL interface from 155–250 kg

1002.73A0 Head rest
1005.50A0 Standard holder
1005.5800 Support arm
Tab. 16: Accessories for NORMAL interface from 155–250 kg
7200.01XX
IFU 7200.01 EN 11 113 / 150
1007.16A0/B0 Head rest adapter

1130.53B0 Head rest
1130.64C0 Head rest
1130.64G0 Head rest
FC/GC
FC/GC
GC
FC/GC
GC
Tab. 16: Accessories for NORMAL interface from 155–250 kg
6.4.4.2 Accessories for REVERSE mounting point 155–250 kg
1002.10A0 Adjustable head rest adapter

1002.73A0 Head rest
1130.53B0 Head rest
1130.64C0 Head rest
Tab. 17: Accessories for REVERSE mounting point 155–250 kg
7200.01XX
114 / 150 IFU 7200.01 EN 11
1130.64G0 Head rest

FC/GC
FC/GC
GC
FC/GC
GC
1433.34AC/FC Carbon fibre back plate for shoulder surgery
6.4.4.3 Accessories for the REVERSE mounting point up to 250 kg, OR table locked (LOCK)
table.
1007.24A1/F1 Universal frame for positioning patients

Tab. 18: Accessories for the REVERSE mounting point up to 250 kg, OR table locked (LOCK)
6.4.5 Maximum overall load 250–454 kg
6.4.5.1 Accessories for NORMAL interface from 250-454 kg
1130.64A0/C0/D0/ Head rest

F0/G0
1130.67A0/B0/C0/F0 Head rest with gas-strut assisted adjustment
FC/GC
Tab. 19: Accessories for NORMAL interface from 250-454 kg
7200.01XX
IFU 7200.01 EN 11 115 / 150
6 Projection

FC/GC
GC
Tab. 19: Accessories for NORMAL interface from 250-454 kg
6.4.5.2 Accessories for REVERSE mounting point 250–454 kg

6.5 Projection
NO TE
If accessories are to be used within table top configurations that are not listed in
this chapter, the accessories can be used taking into account the maximum projec-
tion of the OR table or table top and the maximum weight load of the accessories.
6.5.1 Protrusion with a NORMAL patient orientation
Fig. 91: Protrusion with a NORMAL patient orientation
Maximum protrusion with an overall load of Up to 155 kg to 250 kg to

155 kg 250 kg 454 kg
1 Protrusion at NORMAL mounting point, LOCK 1155 mm 800 mm 540 mm
2 Protrusion at REVERSE mounting point, LOCK 1180 mm 930 mm 675 mm

155 kg 250 kg 454 kg
1 Protrusion at NORMAL mounting point, UN- 800 mm 800 mm -
LOCK
2 Protrusion at REVERSE mounting point, UN- 930 mm 930 mm -
LOCK
7200.01XX
116 / 150 IFU 7200.01 EN 11
Projection 6
6.5.2 Protrusion with a REVERSE patient orientation
Fig. 92: Protrusion with a REVERSE patient orientation

155 kg 250 kg 454 kg
1 Protrusion at NORMAL mounting point, LOCK 1180 mm 930 mm -
2 Protrusion at REVERSE mounting point, LOCK 1155 mm 800 mm -

155 kg 250 kg 454 kg
1 Protrusion at NORMAL mounting point, UN- 1180 mm 930 mm -
LOCK
2 Protrusion at REVERSE mounting point, UN- 800 mm 800 mm -
LOCK
6.5.3 Maximum height with moveable OR table (UNLOCK)
Overall load Maximum height

Up to 155 kg 850 mm (bottom edge of pad)
155 kg to 250 kg 850 mm (bottom edge of pad)
250 kg to 450 kg Approved for lowest position
7200.01XX
IFU 7200.01 EN 11 117 / 150
Display notes
7 Structure of display notes
7 Display notes
7.1 Structure of display notes

If a function is activated on the control device, a note will also appear on the display. The display
note will be hidden again 2 seconds after the selected function is released.
The display notes are divided into three categories:
• Notes on use
• Special notes on use
• Warning notes / Status messages
For better differentiation, the three categories are indicated by an icon and a background colour.
Symbol Meaning
The icon identifies operating notes.
The operating notes are shown with no background colour.
The icon identifies special operating notes.

The special operating notes are shown with a green background colour.
The icon identifies warning notes and status messages.

The warning notes and status messages are shown with an orange background col-
our.
Tab. 21: Structure of display notes
7.2 Notes on use

Notes on operation Comment
Final position reached! −
Central position of longitudinal shift –
reached!
OR table is being initialised The OR table is being configured.
1. Actuate the desired adjustment function again
after the OR table has been started.
Invalid button combination The various adjustment functions cannot be per-
formed simultaneously, e.g. the [Leg up] and the
[Leg down] buttons cannot be pressed simultan-
eously.
Zero-position has been reached (without leg Table top is aligned horizontally except for the leg
plates) plates.
Zero-position reached The table top is aligned horizontally.
Data being transferred The OR table exchanges data with the hand con-
trol.
Setting not supported This message appears when the setting is not
available.
Tab. 22: Notes on operation / special notes on operation
7200.01XX
118 / 150 IFU 7200.01 EN 11
Display notes
Notes on use 7
Notes on operation Comment

Settings saved –
Function not available This message appears when the button has no
function in this configuration of the system.
Operating table lock is active –
Operating table top lock is active –
Lock released –
System is in service mode –
Memory position is not valid Called up patient position has not been defined.
1. Define patient position.
Reading error
1. Inform Getinge Service.
Moves to table position Moves to selected patient position.
Place OR table on its castors (UNLOCK) –
Put down OR table (LOCK) –
Set the correct patient orientation –
Tab. 22: Notes on operation / special notes on operation
7200.01XX
IFU 7200.01 EN 11 119 / 150
Display notes
7 Warning notes / Status messages
7.3 Warning notes / Status messages
NO TE
With every status message, the error code is displayed under the attention symbol.
If the error cannot be corrected, note the error code and forward it to the service
technician authorised by Getinge.
Warning note / Status message Comment

Updating the hand control The software for the control device must be up-
dated.
1. Inform Getinge Service.
Service message for table top 1. Wait five seconds until the hand control
switches off automatically.
2. Select the adjustment function again.
3. If the status message is still shown, notify
Getinge Service.
No connection to OR table 1. Decrease the distance between the IR remote
control and the OR table or change the posi-
tion to the operating table.
Movement stopped 1. Wait five seconds until the hand control
3. If the status message is still shown, make a
note of the error number and notify a Getinge
authorised service technician.
Incompatible software version 1. Inform Getinge Service.
The battery of the IR remote control is 1. Charge the IR remote control in the charging
empty station.
No function with IR Code 00 1. Set the IR code of the IR remote control.
Service message column 1. Wait five seconds until the hand control
note of the error number and notify Getinge
Service.
Recharge the batteries of the column Battery must be recharged.
1. Connect to mains supply.
Tab. 23: Warning notes / Status messages
7200.01XX
120 / 150 IFU 7200.01 EN 11
Display notes
Warning notes / Status messages 7
Warning note / Status message Comment

Service message foot control 1. Wait five seconds until the hand control
note of the error number and notify the
Getinge authorised service centre.
Longitudinal shift is adjusted Depending on the table top position, the longitud-
inal shift will be corrected to prevent collisions.
Press the corresponding multi-function button on
the hand control in order to correct the longitud-
inal shift.
Tab. 23: Warning notes / Status messages
7200.01XX
IFU 7200.01 EN 11 121 / 150
Cleaning and disinfection
8 General information
8 Cleaning and disinfection

The product must be cleaned and disinfected after each use. The product can be wiped down to
disinfect it.
The product can be classified as a non-critical medical device without increased reprocessing re-
quirements.
8.1 General information
DA NG ER !
Risk due to mishandling of cleaning agents and disinfectants!
• The entire cleaning process may only be completed by qualified technicians.
• For information on concentration, temperature and contact and drying times,
refer to the instructions of the detergent and disinfectant manufacturer.
• Observe current national and international regulations for hygiene in the med-
ical field.
• Observe the cleaning and hygiene regulations of the hospital.
DA NG ER !
Risk of infection!
Residues on the product (e.g. blood, secretions etc.) can prevent proper dis-
infection.
• Remove coarse impurities from the product immediately with suitable non-fixing
agents.
• Adjust the cleaning agent to the disinfectant (using a combination agent if ne-
cessary) in order to avoid interactions.
DA NG ER !
Risk of infection!
Product may be contaminated.
• Always wear gloves when cleaning / disinfecting.
• If necessary, take further protective measures.
DA NG ER !
Potentially fatal electrical shock!
• Make sure that the mains connection is disconnected before cleaning and dis-
infection.
• Ensure that no liquids can penetrate any live parts.
DA NG ER !
Risk of explosion!
Agents containing alcohol can form explosive vapour mixtures and ignite
where high-frequency equipment is being used. The cleaning and disinfect-
ing agents must be dried before use.
Ensure that there are no alcoholic residues on the product during high frequency
use.
7200.01XX
122 / 150 IFU 7200.01 EN 11
General information 8
WARN ING !
Risk of injury!
If unsuitable cleaning agents and disinfectants are used, the antistatic prop-
erty and electrical conductivity of the product may be lost, which are re-
quired to prevent electrostatic charges as required by the standard.
Only use detergents and disinfectants of the specified active ingredient groups.
CA UTI ON !
Material damage due to friction and crevice corrosion!
During machine preparation, lubricants are washed out of the joints and
moving parts.
• Lubricate joints and moving parts with appropriate lubricants after preparation.
• Use paraffin oil based lubricants if possible with accessories.
• A lubrication plan can be requested from the responsible Getinge office.
CA UTI ON !
Improper cleaning and disinfection can cause property damage!
• Observe the manufacturer's instructions for concentrations of cleaning agents
and disinfectants
• Perform visual and functional inspections after each cleaning and disinfection
process.
8.1.1 No mechanical preparation
CA UTI ON !
Property damage!
Do not use any mechanical cleaning or disinfection processes.
7200.01XX
IFU 7200.01 EN 11 123 / 150
8 General information
8.1.2 Padding
DA NG ER !
Risk of injury!
The adhesive force of the SFC pad on the product is reduced if the adhesive
tapes of the Velcro fastener on the product are contaminated. The patient
may slip off the OR table if the SFC pad is not secured properly to the sur-
face.
• Remove contamination with a plastic comb.
• After use, prepare the plastic comb with suitable cleaning and disinfecting
agents.
CA UTIO N !
Improper cleaning and disinfection can cause property damage!
Moisture can penetrate damaged padding. Hygiene requirements are then no
longer satisfied.
Replace damaged padding immediately.
NO TE
Remove pads which are removable from the product before cleaning and disinfec-
tion, then only replace them once they have dried.
7200.01XX
124 / 150 IFU 7200.01 EN 11
Cleaning agents and disinfectants 8
8.2 Cleaning agents and disinfectants
8.2.1 Suitable cleaning agents

The cleaning agents must be compatible with the disinfectants used. The use of fixing agents in
the cleaning process such as alcohols or aldehydes should be avoided.
Cleaners with the following properties may be used:
• Slightly alkaline
• Surfactants and phosphates as active cleaning components
8.2.2 Suitable disinfectants

Use only surface disinfectants with the following active ingredient bases for manual disinfection:
Ingredient group Active ingredients

Aldehydes 2-ethyl-1-hexanal, formaldehyde, glutardialdehyde, glyoxal, o-
phthaldialdehyde, succinaldehyde
Guanidine derivatives Alkyl-biguanide, chlorhexidine-digluconate, cocospropylene-diam-
ine guanidinium diacetate, oliogomeric biguanide, polyhexamethyl-
ene biguanide hydrochloride (oligo-diimino imiodo-carbonyl imino-
hexamethylene, polyhexanide)
Quaternary ammonium Alkyl-didecyl-polyoxethyl ammonium propionate, alkyl-dimethyl-al-
compounds kylbenzyl ammonium chloride, alkyl-dimethyl-ethyl ammonium
chloride, alkyl-dimethyl-ethylbenzyl ammonium chloride, benza-
lkonium propionate, benzalkonium chloride (alkyl-dimethyl-benzyl
ammonium chloride, coco-dimethyl-benzyl ammonium chloride,
lauryl-dimethyl-benzyl ammonium chloride, myristyl-dimethyl-ben-
zyl ammonium chloride), benzethonium chloride, benzyl-di-
hydroxyethyl-coco-alkyl ammonium chloride, dialkyl-dimethyl am-
monium chloride (didecyl-dimethyl ammonium chloride), didecyl-
methyl-oxyethyl ammonium propionate, mecetronium-ethyl sulfate,
methyl-benzethonium chloride, n-octyl-dimethyl-benzyl ammonium
chloride
Tab. 24: Active ingredients of disinfectants
8.2.3 Non-usable products / substances

The following products/substances must not be used for cleaning and disinfection:
• Alcohol-based agents (e.g. hand and skin disinfectants)
• Halogenides (e. g. fluorides, chlorides, bromides, iodides)
• Dehalogenating compounds (e. g. fluorine, chlorine, bromine, iodine)
• Products that scratch the surface (e.g. scouring agents, wire brushes, steel wool, cleaning
sponges containing iron)
• Standard commercial solvents (e. g. benzene, thinner)
• Water containing particles of iron
• Products containing acid (e.g. hydrochloric acid)
• Saline solutions
7200.01XX
IFU 7200.01 EN 11 125 / 150
8 Prepare the OR table for cleaning
8.3 Prepare the OR table for cleaning

1. Align the operating table horizontally.
2. Move the operating table to the highest position.
8.4 Manual preparation
CA UTIO N !
Improper cleaning can cause property damage!
Cleaning agents may not be sprayed directly into joints and cracks, and do not use
pressure / steam cleaners!
CA UTIO N !
Improper preparation can cause property damage!
Use soft, lint-free cloths to prepare the product.
8.4.1 Pre-cleaning
In case of heavy soiling it is recommended to pre-clean the product with non-fixing agents.
The following actions are to be carried out as required:

1. Remove dirt with a slightly alkaline cleaner and a soft, lint-free cloth.
2. Thoroughly clean the product with a soft, lint-free cloth moistened with pure water.
8.4.2 Disinfection
1. Select a suitable disinfectant according to the specifications.
2. Use the concentration specified by the disinfectant manufacturer for proper disinfection.
3. Thoroughly wipe the product with a soft, lint-free cloth moistened with disinfectant solution.
4. Make sure that the product is free of impurities.
8.4.3 Drying
Wipe-down disinfection does not require any drying, as excess disinfectant evaporates.
1. Observe the drying time specified by the disinfectant manufacturer.
2. Ensure that only dry padding is attached to the product.
8.4.4 Inspections
1. Carry out visual and functional inspections.
7200.01XX
126 / 150 IFU 7200.01 EN 11
Maintenance
Visual and functional inspections 9
9 Maintenance
9.1 Visual and functional inspections

To ensure correct operation, it is necessary to have visual and functional inspections performed
by a trained person prior to each use.
Documentation of the results of the visual and functional inspections is recommend and should
include the date and signature of the person who performed the inspections. The following table
may be used as a template.
Suggestion:
No. Inspection Defects are present No defects

1 Has the product not been □ 1. Do not continue to use the □
cleaned and disinfected in ac- product.
cordance with hygiene regula-
tions? 2. Clean and disinfect the
product in accordance with
hygiene regulations.
Comment:
2 Is the control panel on the con- □ 1. Notify Getinge authorised □

trol device damaged? service.
Comment:
3 Are the selected adjustment □ 1. Do not continue to use the □

functions not executed? product.
2. Notify Getinge authorised
service.
Comment:
4 Are there fissures in the pad- □ 1. Do not use the padding any □
ding? longer.
Comment:
5 Does the padding no longer ad- □ 1. Do not use the padding any □
here? longer.
Comment:
Tab. 25: Visual and functional inspections
7200.01XX
IFU 7200.01 EN 11 127 / 150
Maintenance
9 Visual and functional inspections
No. Inspection Defects are present No defects

6 Are there damages to mechan- □ 1. Do not continue to use the □
ical parts? product.
service.
Comment:
7 Are there damages to the insu- □ 1. Do not continue to use the □

lation of electrical cables? product.
service.
Comment:
8 Is there any leakage in the □ 1. Do not continue to use the □

product? product.
2. Inform service personnel.
Comment:
9 Is it possible to operate the fol- □ 1. Do not continue to use the □
lowing adjustment functions for product.
the product to the end posi-
tions? 2. Inform service personnel.
▪ Inclining the table top
▪ Tilting the table top laterally
▪ Leg plate segment up / down
▪ Raising / lowering the back
plate
▪ Leg plate (REVERSE back
plate) up / down
▪ Longitudinal shift head/foot
end
Comment:
10 Are the LOCK / UNLOCK func- □ 1. Do not continue to use the □

tions adjustable? product.
2. Inform service personnel.
Comment:
11 (Space for other tests) □ 1. □
Comment:
Tab. 25: Visual and functional inspections
7200.01XX
128 / 150 IFU 7200.01 EN 11
Maintenance
Malfunctions and troubleshooting 9
9.2 Malfunctions and troubleshooting
9.2.1 OR table
No Appearance/Inspection Activity/Rectification/Measure
.
1 The end positions for the motor- 1. Execute the following motorised adjustment
powered adjustment functions have functions to the end position:
not been used over an extended
period of time, causing "play" in the ▪ Inclining the table top
cardan suspension. ▪ Tilting the table top laterally
▪ Moving the table top longitudinally
2 Battery charge status on the override Recharge the OR table batteries:
operating panel flashes red / orange
1. Connect the mains cable to the OR table and
and a warning notice is displayed on
the control device. then to the power socket.
Ø The status display for mains connection on
the override control panel is lit up in green.
Ø The rechargeable battery of the OR table is
being charged.
Tab. 26: Faults and troubleshooting
7200.01XX
IFU 7200.01 EN 11 129 / 150
Maintenance
9 Malfunctions and troubleshooting
.
3 The OR table with autodrive can no If the swivel castors do not extend:
longer be moved.
1. Remove the blindcap (1) on the OR table base.
2. Insert the blind cap on the wrench (2).
3. Insert the other end of the wrench into the
mounting point (3) on the OR table.
1 4. Turn the wrench clockwise (4).
Ø The swivel castors extend.
Ø The wrench can no longer be moved when
2
the swivel castors are fully extended.
4
5. Pull the wrench out of the mounting point on the
3
OR table and the blind cap.
6. Store the wrench in the blind cap and reattach
the blind cap to the base of the OR table.
7. Move the OR table.
8. Inform service personnel immediately.
Please note:
Do not press the [LOCK] button if the castors were
extended with the wrench. Otherwise, the OR table
will be lowered and can no longer be mobilised.
4 The OR table without autodrive can If the swivel castors do not extend:
no longer be moved.
1. Loosen the five screws along the sides of the
OR table base cover.
2. Remove the OR table base cover.
3. Remove the screws from the enclosed pack-
aging in the OR table base.
4. Insert three screws (1) into each swivel castor
and tighten clockwise with a wrench.
Ø The swivel castors extend.
1 Ø The wrench can no longer be moved when
the swivel castors are fully extended.
5. Attach the OR table base cover.
6. Move the OR table.
7. Inform service personnel immediately.
7200.01XX
130 / 150 IFU 7200.01 EN 11
Maintenance
Malfunctions and troubleshooting 9
9.2.2 IR remote control
.
1 Weak transmission power Batteries discharged.
1. Recharge the IR remote control in the charging
unit.
Defective batteries.
1. Have the IR remote control checked by author-
ised service technicians.
7200.01XX
IFU 7200.01 EN 11 131 / 150
Maintenance
9 Inspection and Maintenance
9.3 Inspection and Maintenance

In order to ensure the operational safety of the product, an inspection must be carried out annu-
ally in accordance with the generally recognised rules of technology. The inspection includes
technical safety checks as well as any lubrication of the product. The inspection is to be carried
out by specialist personnel who, on account of their education, knowledge and experiences
gained from practical activities, are capable of correctly executing the technical safety checks.
For the execution of the inspection, technical information is available from Getinge on request.
To ensure availability of all functions as well as an increased service life, Getinge recommends
concluding a maintenance contract. Getinge offers maintenance services at different levels.
Maintenance may only be performed by Getinge Service or service technicians that have been
authorised by Getinge. Maintenance must be performed every 2 years and, as of the 5th year,
every year.
9.4 Maintenance of corded hand controls

This product is maintenance-free.
Wear caused by use and age may influence the safety-relevant functions of the product.
Check the state of the product prior to each use.
If defects are discovered, do not continue to use the product.
Inform the relevant Getinge representative for repairs.
9.5 Repair
A damaged product may not be used and you may not repair it yourself. Please have the follow-
ing information at hand for your Getinge representative:
• Description of the defect
• Product number (see type plate)
• If available: Serial number (see type plate)
• Construction year (see type plate)
Hotline for Germany: +49 (0) 180 32 12 144
Hotlines for other countries can be found at www.getinge.com.
7200.01XX
132 / 150 IFU 7200.01 EN 11
Maintenance
Type plate position 9
9.6 Type plate position

Position of the type plate 1 on the product.
Fig. 93: Type plate position of MEERA OR table

(7200.01)
7200.01XX
IFU 7200.01 EN 11 133 / 150
Maintenance
9 Replacing fuse/setting the mains voltage
9.7 Replacing fuse/setting the mains voltage

The mobile operating table can be set to run on various mains voltages and different fuses will be
required in each case. Use the following fuses:
• 100–127 V: T2.5AH 250 V 5×20 mm (0217.0894)
• 200-240 V: T1.6AH 250 V 5×20 mm (0217.0884)
1. Ensure that the mains plug is disconnec-

ted.
2. When operating the mobile operating table
in battery-powered mode, use the [ON]
and [UP] buttons on the override panel to
set it to the highest position.
1
3. Undo the fuse insert (1) with a screwdriver

or a coin.
4. Remove the fuse insert.
Fig. 94: Inserting/removing the fuse
1. Open the cover of the transformer com-

partment (2).
4
2. Use a screwdriver (min. blade width
11
5 240 100 10 mm) to set the selector switch (3) for
2
22
127 200
the desired voltage range (4):

• For mains voltage 110-120 V: Select
3 115 V
• For mains voltage 230-240 V: Select
240 V
• Other voltage: Select the appropriate
voltage range
3. Install a fuse suitable for the set voltage
and ensure it is fitted correctly.
4. Ensure that the fuse used matches the set
voltage.
Fig. 95: Setting the mains voltage 5. Close the transformer compartment cover.
7200.01XX
134 / 150 IFU 7200.01 EN 11
Technical specifications
General specifications 10
10 Technical specifications
NO TE
For dimensions, adjustment ranges and weight specifications, there is a tolerance
of ±5 %, if no other tolerance is specified.
10.1 General specifications

Type of protection against electric shock Protection class II
Level of protection against electrical shock Table top: Type B (IEC 60601-1)
Risk of explosion Class AP (for battery operation)
Protection against ingress of liquids IP X4 (spray water protection)
10.2 Ambient conditions

Temperature: Shipping / storage -20 °C to +50 °C
Temperature: Operation +10 °C to +40 °C
Relative humidity: Shipping / storage 10 % to 95 %
Relative humidity: Operation 30 % to 75 %
(non-condensing)
Atmospheric pressure: Shipping / storage 500 hPa to 1060 hPa
Atmospheric pressure: Operation 700 hPa to 1060 hPa
10.3 Surface temperature of application set

Maximum surface temperature of application set 45 °C
10.4 Noise level

Noise level approximately 53 dB (A)
10.5 Electrical specifications

Nominal voltage AC 127 / 200 / 120 / 240 / 100 / 220 V
Nominal frequency 50 / 60 Hz
Power consumption maximum 230 VA
Internal operating voltage IPS SELV DC 24 V
Operating mode int 10 min on / 20 min off
With an overall load as of 250 kg:
int 2 min on / 120 min off
Rechargeable batteries 2 each with 12 V / 18 Ah
7200.01XX
IFU 7200.01 EN 11 135 / 150
10 Weight
10.6 Weight
Net weight 291 kg
10.7 Dimensions
Fig. 96: Dimensions
Length of basic table top 860 mm ±5 mm

Width of basic table top 540 mm ±5 mm
Width of basic table top with side rails 590 mm ±5 mm
Height (without pad) 600-1050 mm ±10 mm
7200.01XX
136 / 150 IFU 7200.01 EN 11
Adjustment ranges 10
10.8 Adjustment ranges
10.8.1 Longitudinal shift
Fig. 97: Longitudinal shift
Longitudinal shift towards the head end 155 mm ±10 mm

Longitudinal shift towards the foot end 155 mm ±10 mm
10.8.2 Inclination
Fig. 98: Inclination
Inclination, Trendelenburg 25° ±3°

Inclination, reverse Trendelenburg 35° ±3°
7200.01XX
IFU 7200.01 EN 11 137 / 150
10 Adjustment ranges
10.8.3 Tilt
Fig. 99: Lateral tilt
Tilt to the left 20° ± 2°

Tilt to the right 20° ± 2°
10.8.4 Back plate
Fig. 100: Adjustment angle of back plate, NORMAL mounting point
Back plate, up 70° ± 5°

Back plate, down 40° ± 4°
7200.01XX
138 / 150 IFU 7200.01 EN 11
Adjustment ranges 10
80°
90°
Fig. 101: Adjustment angle of back plate, REVERSE mounting point
Back plate, up 80° ±5°

Back plate, down 90° ±5°
10.8.5 Leg plate
Fig. 102: Adjustment angle of leg plate, REVERSE mounting point
Leg plate, up 80° ± 5°

Leg plate, down 90° ± 5°
7200.01XX
IFU 7200.01 EN 11 139 / 150
10 Table top positions
10.9 Table top positions
10.9.1 FLEX position
Fig. 103: FLEX position, NORMAL patient orientation
FLEX position 40° ± 5°

Inclination, reverse Trendelenburg 20° ± 5°
Fig. 104: FLEX position, REVERSE patient orientation
FLEX position 40° ± 5°

Inclination, reverse Trendelenburg 20° ± 5°
7200.01XX
140 / 150 IFU 7200.01 EN 11
Table top positions 10
10.9.2 REFLEX position
Fig. 105: REFLEX position, NORMAL patient orientation
REFLEX position 40° ± 5°

Inclination, Trendelenburg 20° ± 5°
Fig. 106: REFLEX position, REVERSE patient orientation
REFLEX position 40° ± 5°

7200.01XX
IFU 7200.01 EN 11 141 / 150
10 Table top positions
10.9.3 BEACH CHAIR position
20°
40°
20°
Fig. 107: BEACH CHAIR position, NORMAL patient orientation

20° 40°
20°
Fig. 108: BEACH CHAIR position, REVERSE patient orientation

7200.01XX
142 / 150 IFU 7200.01 EN 11
Electromagnetic compatibility (EMC) 10
10.10 Electromagnetic compatibility (EMC)

The product is designed for operation in the environments specified in the intended use. The user
must ensure that the product is operated in such an environment.
10.10.1 Cable lengths

Only cables with the following maximum lengths may be used:
Designation Cable length

Mains cable between the OR table and mains connection 4.5 m
Control cable between the OR table and corded hand control 7m
Control cable between the OR table and foot switch 2.3 m
10.10.2 Electromagnetic emissions
Measurement / Standard Compliance

HF emissions CISPR 11 Group 1
Class A
IEC 60601-1-2 Conformity without deviations
10.10.3 Resistance to electromagnetic interference
Test / Standard Test level

Interference immunity to electrostatic dis- ±8 kV contact discharge
charge (ESD) ±2 kV, ±4 kV, ±8 kV, ±15 kV air discharge
IEC 61000-4-2
Interference immunity to high-frequency 3 V/m
electromagnetic fields 80 MHz – 2.7 GHz
IEC 61000-4-3 80 % AM at 1 kHz
7200.01XX
IFU 7200.01 EN 11 143 / 150
10 Electromagnetic compatibility (EMC)

Interference immunity to near fields from Fre- Radio service Test level
wireless HF communication devices quency (V/m)
IEC 61000-4-3 (MHz)
385 TETRA 400 27
450 GMRS 460 28
FRS 460
710 LTE Band 13 / 17 9
745
780
810 GSM 800 / 900 28
TETRA 800
870
iDEN 820
930 CDMA 850
LTE Band 5
1720 GSM 1800 28
CDMA 1900
1845
GSM 1900
1970 DECT
LTE Band 1 / 3 / 4 / 25
UMTS
2450 Bluetooth 28
WLAN 802.11 b / g / n
RFID 2450
LTE V7
5240 WLAN 802.11 a / n 9
5500
5785
Interference immunity to quick transient ±2 kV for mains cables
electrical disruptions / bursts ±1 kV for input and output cables
IEC 61000-4-4 100 kHz repetition frequency
Interference immunity to surge voltage ±0.5 kV, ±1kV
between lines
IEC 61000-4-5
Interference immunity to surge voltage ±0.5 kV, ±1kV, ±2kV
between line and ground
IEC 61000-4-5
Interference immunity to conducted dis- 3V
turbances, induced by high-frequency 150 kHz – 80 MHz
fields 6 V for ISM bands between 150 kHz – 80 MHz
IEC 61000-4-6 80 % AM at 1 kHz
Interference immunity to magnetic fields 30 A/m

with energy technology frequencies 50 Hz
IEC 61000-4-8
7200.01XX
144 / 150 IFU 7200.01 EN 11
Electromagnetic compatibility (EMC) 10

EMC interference immunity to voltage 0 % UT; 1/2 period
drops, brief interruptions and voltage fluc- At 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°
tuations
0 % UT*; 1 period
IEC 61000-4-11 and
70 % UT; 25/30 periods
Single phase: at 0°
0 % UT; 250/300 periods
7200.01XX
IFU 7200.01 EN 11 145 / 150
Index
A D
Abbreviations 9 Definition
Accessories 23 applied part 16
Side rail 110 Caution 11
Accessory weights 29 CENTRAL position 15
Air humidity 135 Coordinate system 12
Ambient conditions 135 Danger 11
AP-M zone 13 Environment 11
Applicable standards 23 Inclination 12
applied part 16 Lateral tilt 12
Area with a risk of explosions Note 11
AP-M zone 13 Protrusion 13
Atmospheric pressure 135 Warning 11
Autodrive 76, 77 Descriptor 11
Dimensions 136
Directions for use 90
B Disinfectant 125
Batteries Disinfection 122
disposal 20 Disposal
Batteries 20
C Cleaning and disinfection 20
Packing 20
CENTRAL position 15, 90
Pad 20
Charge batteries 75
Product 20
Cleaning 122
Rechargeable battery 20
Cleaning agents 125
Control device
Mounting 39 E
Control devices 24 Electrical specifications 135
Corded control devices Equipotential bonding 72
Connect 41 Extension plate 83
Removing 41
F
Foot switch 42
H
Horizontal alignment
Patient 51
Hydraulic oil
Air bubbles 37
I
Inclination 12, 137
head down 48
Reverse Trendelenburg 48
Initial operation 33
Inspection 132
IR code
display 57
Groupings 36
Identification 36
7200.01XX
146 / 150 IFU 7200.01 EN 11
Index
L R
Lateral tilt 12, 49, 138 Rechargeable battery
Latex-free 24 disposal 20
Leg plate 85, 86 Repair 132
LEVEL 51 Reverse Trendelenburg 12
Longitudinal 12 Trendelenburg 12
Risk of explosion 27, 34, 75
M
Main menu 54 S
Mains operation 75 Sagittal 12
Mains power cable 75 Seat plate extension 84
Maintenance 132 Service interface
Malfunctions 129 Connection 34
Signals
acoustic (OR table) 71
N Software version 60
Noise level 135 Special notes on use 118
Notes on use 118 Standards 23
Status messages 120
O Status reports
Error reports 118
Operating table
Notes on use 118
connect 54
Warning notes 118
OR table
Surface temperature 135
disconnect 57
Symbols 17
Lowering 45
System information
Raising 45
open 60
overall load 87
Permitted 13, 27
T
P Table top
Lateral tilt 49
Packing 20
Longitudinal shift 50
Patient
Table top configurations
Horizontal alignment 51
Overall load 155 kg to 250 kg 101
Patient orientation
Overall load 250 kg to 450 kg 108
Adjusting 61
Overall load of up to 155kg 93
Definition 14
Temperature 135
Patient position
Transport position 13
edit 66
Transverse 12
preset 63
Trendelenburg 12
quick-save 67
Reverse Trendelenburg 12
Save 64
Troubleshooting 129
Select 63, 65
user-defined 64
Permitted overall load 13 U
Pictogram 11 Used electrical devices 20
Positioning position 13
Preparation 123
Protrusion 13 V
Visual and functional inspections 127
7200.01XX
IFU 7200.01 EN 11 147 / 150
Index
W
Warning notes 120
Weight
Accessories 29
Maximum permitted overall load: 27
Net weight 136
Overall load 87
7200.01XX
148 / 150 IFU 7200.01 EN 11
Notes
MAQUET GmbH · Kehler Str. 31 · 76437 Rastatt · GERMANY · Phone: +49 7222 932 -0
www.getinge.com
IFU 7200.01 EN 11 2020-03-03

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Instructions for use

IFU 7200.01 EN 11 2020-03-03

Subject to technical modification!

2.4 Safety notes regarding service ............................................................................................................. 30

3 Initial operation ........................................................................................................ 33

4 Hand controls and functions .................................................................................. 38

4.7.4.4 Disconnect the OR table ..................................................................................... 57

5 Operation and use.................................................................................................... 70

5.3.6.1 Mounting / removing the X-ray top ...................................................................... 88

6 Approved accessories and table top configuration ............................................. 91

7 Display notes............................................................................................................ 118

7.3 Warning notes / Status messages ........................................................................................................ 120

8 Cleaning and disinfection ....................................................................................... 122

9 Maintenance ............................................................................................................. 127

10 Technical specifications.......................................................................................... 135

10.9.3 BEACH CHAIR position ......................................................................................................... 142

1.1 How to use these operating instructions

1.1.2 Symbols and formatting

1.1.3.1 Design of safety notes

Pictogram Descriptor Text

WARNING! Identifies a potential danger to people or property, which

CAUTION! Identifies a potential danger to property, which may res-

Tab. 2: Design of safety notes

1.1.3.2 Structure of notes

Pictogram Descriptor Explanation

ENVIRONMENT Information regarding proper disposal.

Tab. 3: Structure of notes

1.1.3.3 Definition for 3-dimensional coordinate system

Reference X axis Y axis Z axis

Fig. 1: Definition of terms for the 3-dimensional coordinate system

1 Frontal plane (horizontal plane) 3 Transverse plane

1.1.3.4 Definition of inclination and tilt

Fig. 2: Definition of inclination and tilt

1 Reverse Trendelenburg 3 Lateral tilt

1.1.3.5 Definition of hazardous location, Zone AP-M

Fig. 3: Area with a risk of explosions, AP-M zone

1.1.3.6 Definition of permitted overall load

1.1.3.7 Definition of protrusion

1.1.3.8 Definition Positioning- / Transporting

1.1.3.9 Definition of usage-related restrictions

1.1.3.10 Definition of patient orientation

NORMAL patient orientation

The upper part of the patient's body is located

Fig. 4: NORMAL patient orientation

REVERSE patient orientation

The legs are located above the longer section

Fig. 5: REVERSE patient orientation

1.1.3.11 Definition of CENTRAL position

Fig. 6: CENTRAL position

1.1.3.12 Definition of applied part

Fig. 7: Applied part, OR table: Table top

The applied part of the OR table is the table top.

1.2 Symbols used

UL classification mark from Underwriters Laboratories as proof that the

Labelling in accordance with the ISO 15223-1 standard.

Symbol for the labelling of medical devices

Labelling in accordance with the standard ISO 15223-1.

Labelling in accordance with the ISO 15223-1 standard.

Marking according to the standard ISO 15223-1.