Vidia Port

Instructions for use
VidiaPort
Carrying Arm
Read the instructions for use before using the product and ENGLISH
retain for later reference. en-GB
This page is left intentionally blank.
VidiaPort
Manufacturer TRUMPF Medizin Systeme GmbH + Co. KG

Carl-Zeiss-Straße 7-9
07318 Saalfeld
Germany
Telephone: +49 3671 586-0
Fax: +49 3671 586-41165
surgical@hillrom.com
hillrom.com
TRUMPF Medizin Systeme GmbH + Co. KG is a company of the
Hill-Rom Holdings Group. The manufacturer is hereinafter
referred to as Trumpf Medizin Systeme.
Authorised Australian Sponsor Trumpf Med (Aust) Pty Ltd

Unit 4.01, 2-4 Lyonpark Road
Macquarie Park NSW 2113
Phone: +1 800 650 083
Technical Customer Service The contact details for the current sites of the Technical Customer
Service in the individual countries are listed on the Internet at
hillrom.com.
Information about the document Original instructions for use

Document number: 7990089
Language ID: 002
Version: 01
Material number: 2079217
Date of publication: 2021-11-12
The instructions for use are in print format and form part of the
product delivery scope.
This document applies to the following sales units:
Designation Material
number
Support arm system
VidiaPort Ceiling Single 4028110
VidiaPort Ceiling Duo 4028210
VidiaPort Ceiling Trio 4028310
VidiaPort Wall 4028130
VidiaPort Pendant 4028140
VidiaPort Springarm bottom 4028150
VidiaPort Springarm middle 4028152
VidiaPort Springarm top 4028155
Other applicable documents The products listed are individually combined with various
Trumpf Medizin Systeme products. Chapter 2.2 lists the
compatible products and their associated instructions for use. The
instructions for use for all products used apply.
7990089_002_01 – 2079217 – 2021-11-12 3

VidiaPort
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VidiaPort
Basic information
After purchasing, the product is correctly and professionally handed over to the operator. The handover
is carried out by a person authorised by the manufacturer and is documented with the aid of a handover
report.
On delivery, the packaging should be checked for any transport damage. In the event of damage, please
contact the Technical Customer Service before unpacking.
Ensure that you are familiar with the adjustment options and the operation of the product before using
it. Pay attention to the signs on the product.
About these instructions for use
– The instructions for use contain important information on the safe and effective use of the product.
– The instructions for use are part of the product and must be followed.
– Read the instructions for use carefully and in full before using the product. The instructions for use
must be properly understood. If anything is unclear, or if any questions arise about the product,
please contact the manufacturer.
– The instructions for use must be passed on in case of relocation or change of personnel.
– The instructions for use must be available at the place where the product is used.
– The instructions for use must be fully accessible to all users of the product at any time.
– The diagrams in the instructions for use are a simplified version for basic comprehension.
– Residual risks that may occur when handling the product are identified in the document using a signal
word. The necessary safety measures and possible risks are listed if they are not observed. A
corresponding signal word identifies the severity of the risk:
Signal word Meaning

DANGER This signal word denotes a dangerous situation that will lead to immediate death
or severe injury, unless precautionary measures are taken.
WARNING This signal word denotes a dangerous situation that may lead to death or severe
injury, unless precautionary measures are taken.
CAUTION This signal word denotes a dangerous situation that may lead to moderate or
slight injury, unless precautionary measures are taken.
NOTICE This signal word denotes a situation that may lead to product or environmental
damage, unless precautionary measures are taken.
© TRUMPF Medizin Systeme GmbH + Co. KG

Reprinting, copying, or translating this document, in whole or in part, is prohibited without the express
written permission of Trumpf Medizin Systeme. All rights under the copyright laws are expressly
reserved by Trumpf Medizin Systeme.
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VidiaPort
6 7990089_002_01 – 2079217 – 2021-11-12

Contents
Contents
1 Usage specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.1 Intended purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.2 Contraindication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.3 Patient definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.4 User definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.5 Use environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.6 Storage and transport conditions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.7 Service life . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
2 Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
2.1 Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
2.2 Combination with other Trumpf Medizin Systeme products . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
2.3 Combination with products of other manufacturers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
2.4 Responsibility of the operator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
2.5 Signs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
2.5.1 Safety instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
2.5.2 Location and meaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
3 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
4 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
4.1 VidiaPort Ceiling Single support arm system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
4.2 VidiaPort Ceiling Duo support arm system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
4.3 VidiaPort Ceiling Trio support arm system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
4.4 VidiaPort Wall support arm system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
4.5 VidiaPort Pendant support arm system. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
4.6 VidiaPort support arm system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
4.7 Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
4.7.1 Adapter. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
4.7.2 Camera bracket . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
4.7.3 Monitor mount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
4.7.4 Handle adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
4.8 Working range . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
5 Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .29
5.1 Safety instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
5.2 Inspections during operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
5.3 Connecting the power supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
5.4 Disconnecting the power supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
5.5 Attaching the handle adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
5.6 Remove the handle adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
5.7 Positioning the component on the spring arm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
5.8 Adjusting the braking force at the boom and spring arm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
5.8.1 C-boom. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
5.8.2 S-boom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
5.8.3 Spring arm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
5.9 Adjusting the spring force on the spring arm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
5.10 Adjusting the swivel range of the control arm upwards and downwards. . . . . . . . . . . . . . . . 39
5.10.1 Spring arm L21, MD21+, MD26+, MD40+ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
5.10.2 Spring arm LCH19 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
5.11 Adjusting the optional brakes on the spring arm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
5.11.1 Spring arm L21, MD21+, MD26+, MD40+ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
5.11.2 Spring arm LCH19 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
5.12 Setting the braking force on the components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
5.12.1 Monitor mount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
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Contents
5.12.2 Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
5.12.3 Camera bracket . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .46
5.13 Maximum load . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .46
5.14 Decommissioning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
6 Cleaning and disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

6.1 Recommended disinfectants . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .49
6.2 Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .50
6.3 Cleaning and disinfection of the VidiaPort support arm system . . . . . . . . . . . . . . . . . . . . . . . . 51
6.3.1 Wipe disinfection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
7 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53
8 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53
9 Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
10 Spare parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
11 Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55
12 Technical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .56

12.1 Device data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
12.2 Load bearing capacities. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
12.2.1 Boom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
12.2.2 Spring arm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
12.3 SVHC (Substance of very high concern) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
13 Product certification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
13.1 European Union. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .66
13.2 USA/Canada. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .66
13.3 Ukraine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .66
13.4 Serbia . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .66
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Usage specifications
1 Usage specifications
1.1 Intended purpose

The device is intended to carry additional supporting devices
(e.g. monitor).
1.2 Contraindication
No contraindications are known.
1.3 Patient definition

No direct contact or interaction with the patients.
1.4 User definition

The users are persons who are authorized to use and work with
the device. Users can be e.g. non-sterile or sterile OR staff, like a
nurse or a surgeon, cleaning staff and service, maintenance and
hospital technicians.
1.5 Use environment
Temperature: +10 °C to +40 °C / 50 °F to 104 °F

Humidity: 30 % to 75 %
Air pressure: 70 kPa to 106 kPa / 10 psi to 15 psi
Operating height: up to 3,000 m / 9,843 ft above sea level
1.6 Storage and transport conditions
Temperature: -15 °C to +40 °C / 50 °F to 104 °F
Humidity: 5 % to 95 %
Air pressure: 70 kPa to 106 kPa / 10 psi to 15 psi
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Safety
Fragile packaged goods
Top
Protect against moisture
1.7 Service life

The service lifetime is 10 years, if used normally.
2 Safety
2.1 Configuration
The configuration of a boom with the listed products has been
tested by Trumpf Medizin Systeme and subjected to a compliance
assessment.
Spring arm
number
L21, 9P Springarm 2077411
LCH19, 9P Springarm 2077413
MD21+, WS Springarm 2077407
Camera bracket
number
TruVidia Camera Yoke 2077993
Adapter
number
VidiaPort Adapter VESA 100 2077992
Cable port handle 2082139
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Safety
Monitor mount Designation Material

number
VidiaPort Monitor Holder Single 2078861
VidiaPort Monitor Holder Duo 2078862
VidiaPort Monitor Holder Box 2078863
Handle adapter
number
Adaption Standard handle 2065945
Adaption disposable handle 2066135
2.2 Combination with other Trumpf Medizin Systeme products

Trumpf Medizin Systeme offers a variety of products for further
attachment to the support arms. Not all products are available in
all countries. Detailed information is available from the individual
Trumpf Medizin Systeme branches, which can be found
worldwide. Contact details are available online at hillrom.com.
The support arms may be used in combination with the following
Trumpf Medizin Systeme products. The products are described in
separate instructions for use, which users must read carefully and
in full. The document number of the instructions for use is listed in
the right column.
Pre-assembly set
Designation Material Document
number number
Pre-Install Set VidiaPort 4028051 7990000
Supply unit
number number
FCS 300 Electro Cube 1971846 7990082
FCS 700 Ceiling Supply Unit Solo/ 4037210 7990001
TanPrep
TruPort Ceiling Mounted Support 55000-00001
System
FCS 700 Ceiling Supply Unit 4037220 7990001
TanAdd
TruPort Ceiling Mounted Support 55000-00001
System
FCS 500 Ceiling Carrier ML Solo/ 4037251 7990002
TanPrep
FCS 500 Ceiling Carrier ML 4037252 7990002
TanAdd
FCS 500 Ceiling Carrier HL Solo/ 4037261 7990002
TanPrep
FCS 500 Ceiling Carrier HL 4037262 7990002
TanAdd
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Safety
Surgical light Designation Material Document

number number
iLED 7 Ceiling Duo 4068210 7990004
iLED 7 Ceiling Trio 4068310 7990004
iLED 7 Ceiling Quad 4068410 7990004
TruLight 5000/3000 Ceiling Duo 4038210 7990005
TruLight 5000/3000 Ceiling Trio 4038310 7990005
TruLight 5000/3000 Ceiling Quad 4038410 7990005
Camera
number number
TruVidia HD 2000 2072249 7990006
TruVidia HD 5000 2072520 7990006
TruVidia HD 7500 2072521 7990006
Sterilisable handle
number number
Sterilisable Central Handle, 3 pcs 4025708 7990009
Sterilisable Camera Handle, 3 pcs 4025709 7990009
2.3 Combination with products of other manufacturers

The support arms may be operated in combination with the
following MAVIG products.
Designation Manufacturer Material

Material number
number
E-OT25B05 Portegra 2 E-OT25B05 2005395
Radiation Protection 76x60
FA102-TR spring arm FA102-TR 1982310
E-OT54B01-TR Portegra 2 E-OT54B01-TR 2005442
Radiation Protection 78x90
FA402-TR spring arm FA402-TR 1982311
The support arms may be operated in combination with the

following Foreseeson products.
number
Medical Display 24" FSN 2069887
26" HD Medical Display FSN 2069889
32” High-Bright LED Medical Display 2068217
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Safety
The support arms are not intended for use with products of other
manufacturers (third-party products) and where Trumpf Medizin
Systeme has not conducted any compatibility tests. However,
Trumpf Medizin Systeme does not exclude the possibility of use
with third-party products. If the operator intends to combine the
support arm system with third-party products, the operator is
responsible for this combination. Trumpf Medizin Systeme does
not take any responsibility for the combination of the support
arms with third-party products. The guarantee/warranty for
Trumpf Medizin Systeme products may become void if they are
combined with third-party products.
2.4 Responsibility of the operator

The operator is the natural or legal person who directly operates
the product for commercial or economic purposes or allows a
third party to use it. The operator has legal product responsibility
regarding the protection of personnel or third parties.
The medical devices may only be operated and used according to
their intended purpose and the general rules of technology.
Medical devices may only be used by persons who have the
training or knowledge required to do this.
Training on the proper handling of the medical device is required.
However, training is not required when the medical device is self-
explanatory or when instructions for a product with the same
design have already been provided.
Interconnected medical products, as well as those combined with
accessories, including software or other objects, may be operated
and used only if they are suitable for use in this combination,
taking into account their intended purpose and the safety of
patients, users, employees or third parties.
Before the medical device is applied, the user must ensure that the
product is operational and in an appropriate state and the user
must further have read the instructions for use as well as other,
attached, safety-relevant information and maintenance
instructions.
The instructions for use and the instructions provided with the
medical device must be stored in a way that ensures that the user
can access the information required for using the medical device
at any time.
The user and/or patient must report any serious incidents related
to the use of the medical device to the manufacturer and the
relevant authorities of the member state of which the user and/or
the patient is a resident.
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Safety
2.5 Signs
2.5.1 Safety instructions
– Signs on the product inform about residual risks during use or

provide useful additional information.
– The device label and all signs must be undamaged and
attached at the specified locations on the product. A damaged,
illegible or missing device label/sign must always be replaced.
– Pay attention to the signs on the product.
– Signs may not be changed or removed.
2.5.2 Location and meaning
D B A
C E D
D
D
D D
B
No. Sign Meaning

[A] Observe the instructions for use
[B] Manufacturer’s logo
[C] not available –
14 7990089_002_01 – 2079217 – 2021-11-12

Safety
No. Sign Meaning

[D] Device label for the individual component
[E] Device label for the support arm system
Manufacturer
Unique Device Identification (UDI) comprising:

– Data Matrix Code
– (01) Global Trade Item Number (GTIN)
– (11) Date of manufacture (year/month/day)
– (21) Serial number
– (240) Material number
Trumpf Medizin Systeme material number
Serial number
Medical device
Product is declared compliant with Regulation 2017/745/EU

concerning medical devices.
The product must be disposed of in accordance with the
requirements of Directive 2012/19/EU on WEEE II and relevant
national regulations at a suitable waste disposal point for the
recycling of electrical and electronic devices.
Caution! Note the warning information in the Instructions for
Use!
Manufacturing date
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Overview
3 Overview
The VidiaPort is a modular configurable support arm system.
Different variants are available:
VidiaPort Ceiling Single/Duo/Trio

– mounted on a ceiling conduit
– with a central axis with at most 3 extension arms
The central axis serves as a carrier system for the
VidiaPort Ceiling support arm system.
– with one spring arm per boom
VidiaPort Wall
– mounted on a wall bearing
The wall bearing is used as a holder for the VidiaPort Wall
support arm system.
– with an extension arm (reduced load capacity)
– with one spring arm
VidiaPort Pendant
– in combination with a monitor support FCS 500 or with a
FCS 700/TruPort ceiling-mounted supply unit
– mounted on the Pendant Adapter of the FCS/TruPort
– with an extension arm (reduced load capacity)
– with one spring arm
Various monitor mounts (maximum 2 flat screens on a monitor

mount), camera brackets or other devices can be mounted on the
support arm system.
There are 2 versions of booms:

– C-boom
– S-boom
A C-boom has a higher maximum additional load and is available in
larger boom lengths than an S-boom. The cross-section for the
cable ducts is greater than for the S-booms.
The S-boom and C-boom can be combined with each other.
A maximum of 4 booms (2 C-booms and 2 S-booms) can be

mounted on a central axis in combination with a surgical lighting
system. Up to 3 S-booms can be installed on a central axis of the
S variant.
On the central axis in a support arm system with different boom
versions, the C-booms, with a maximum of 2 in a support arm
system, are always installed above the S-booms.
The VidiaPort Bottom, Middle and Top Springarms are used on
support arm systems in combination with surgical lights.
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Description
4 Description
VidiaPort support arm systems are available as Single, Duo, Trio,
Wall and Pendant versions with varying boom lengths and
accessory components. Monitor mounts or other devices can be
assembled on the support arms.
The VidiaPort Bottom, Middle and Top Springarms are only
available in combination with a TruLight 5000/3000 or an iLED 7
surgical light system. Up to three VidiaPort Springarms (Bottom,
Middle or Top) can be mounted on this support arm system. The
support arm systems are described and depicted in the user
instructions of the surgical light system.
4.1 VidiaPort Ceiling Single support arm system

The VidiaPort Ceiling Single support arm system used here as an
example consists of the following components:
– the canopy [16]
– the ceiling pipe [1] (a part of the Pre-Install Set VidiaPort) and
the central axis [2]
– a lower, horizontally rotating boom [3] on the central axis [2]
with horizontally and vertically adjustable MD40+ spring arm [7]
– a monitor mount (VidiaPort Monitor Holder Duo) [5] at the
boom for attaching two flat screen monitors
The example of the VidiaPort Ceiling Single support arm system is
supplemented with the following accessories of Trumpf Medizin
Systeme and the following third-party products:
– two sterilisable handles [8] at the monitor mount [5]
– two medical flat screen monitors [11] (products from third-party
manufacturers)
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Description
16
1
3
8 8
11 11
[1] Ceiling conduit

[2] Central axis
[3] Boom
[5] Monitor mount
(VidiaPort monitor Holder Duo and VidiaPort monitor Holder
Box)
[7] Spring arm
(MD40+)
[8] Sterilisable handle
(Sterilisable Central Handle, 3 pcs)
[11] Flat screen
[16] Canopy
4.2 VidiaPort Ceiling Duo support arm system

The VidiaPort Ceiling Duo support arm system used here as an
– the canopy [16]
– an upper, horizontally rotating boom [3] on the central axis [2]
with horizontally and vertically adjustable L21+ spring arm [12]
upper boom for attaching two flat screen monitors
The example of the VidiaPort Ceiling Duo support arm system is
– one camera bracket (TruVidia Camera Yoke) [6] in combination
with TruVidia camera system [9] or handle adapter [10] on the
lower boom
– two sterilisable handles [8] at the monitor mount [5]
– one sterilisable handle [8] for the TruVidia [9] camera system or
the handle adapter [10]
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Description

manufacturers)
16
1
3
4
2
7
12
6
5
8 8 10
9
8 8
11 11
[1] Ceiling conduit

[2] Central axis
[3] Upper boom
[4] Lower boom
[5] Monitor mount
Box)
[6] Camera bracket
(TruVidia Camera Yoke)
[7] Spring arm
(MD40+)
(Sterilisable Central Handle, 3 pcs/Sterilisable Camera
Handle, 3 pcs)
[9] Camera
(TruVidia HD)
Only use the camera with the sterilisable handle [8].
[10] Handle adapter
(Adaption Standard handle/Adaption disposable handle)
[11] Flat screen
[12] Spring arm
(L21)
[16] Canopy
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Description
4.3 VidiaPort Ceiling Trio support arm system

The VidiaPort Ceiling Trio support arm system used here as an
– the canopy [16]
– a middle, horizontally rotating boom [13] on the central axis [2]
with horizontally and vertically adjustable L21+ spring arm [12]
upper boom for attaching two flat screen monitors
– a monitor mount (VidiaPort Monitor Holder Single) [15] at the
middle boom for attaching one flat screen monitor
The example of the VidiaPort Ceiling Trio support arm system is
supplemented with the following Trumpf Medizin Systeme
accessories and the following third-party products:
– one camera bracket (TruVidia Camera Yoke) [6] in combination
with TruVidia camera system [9] or handle adapter [10] on the
lower boom
– one sterilisable handle [8] for the TruVidia [9] camera system or
the handle adapter [10]
– three medical flat screen monitors [11] (products from third-
party manufacturers)
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Description
16 1
3
4
13
7 2
14
12
5
6
15
8 8
8 10
9
11 11
8 8
11
[1] Ceiling conduit

[2] Central axis
[3] Upper boom
[4] Lower boom
[5] Monitor mount
Box)
[6] Camera bracket
(TruVidia Camera Yoke)
[7] Spring arm
(MD40+)
(Sterilisable Central Handle, 3 pcs/Sterilisable Camera
Handle, 3 pcs)
[9] Camera
(TruVidia HD)
Only use the camera with the sterilisable handle [8].
[10] Handle adapter
(Adaption Standard handle/Adaption disposable handle)
[11] Flat screen
[12] Spring arm
(L21)
[13] Middle boom
[14] Spring arm
(MD21+)
[15] Monitor mount
(VidiaPort monitor Holder Single and VidiaPort Monitor
Holder Box)
[16] Canopy
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Description
4.4 VidiaPort Wall support arm system

The VidiaPort Wall support arm system used here as an example
consists of the following components:
– the wall bearing [17]
– a horizontally rotating boom [3] on the wall support [17] with
horizontally and vertically adjustable MD21+ spring arm [14]
boom for attaching one flat screen monitor
The example of the VidiaPort Wall support arm system is
– one sterilisable handle [8] at the monitor mount [15]
– a medical flat screen [11] (product of third-party manufacturer)
3
17
14
15
11
[3] Boom
[11] Flat screen
[14] Spring arm
(MD21+)
[15] Monitor mount
Holder Box)
[17] Wall support
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Description
4.5 VidiaPort Pendant support arm system

The VidiaPort Pendant support arm system used here as an
– the canopy [16]
– of the ceiling-mounted supply unit FCS/TruPort [18] with a
Pendant Adapter [19]
– a horizontally rotating boom [3] on the Pendant Adapter [19]
boom for attaching one flat screen monitor
The example of the VidiaPort Pendant support arm system is
supplemented with the following Trumpf Medizin Systeme
accessories and the following third-party products:
– one sterilisable handle [8] at the monitor mount [15]
manufacturers)
18
16
11
19
3
14
15
11
[3] Boom
[11] Flat screen
[14] Spring arm
(MD21+)
[15] Monitor mount
Holder Box)
[16] Canopy
[18] Ceiling-mounted supply unit FCS 700 Ceiling Supply Unit/
TruPort Ceiling Mounted Support System
[19] Pendant Adapter
(light adaptation at the ceiling-mounted supply unit)
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Description
4.6 VidiaPort support arm system

The following arm lengths can be installed on the central axis:
Boom length [A] S-boom C-boom
2,250 mm / 88.58 inch – x
2,100 mm / 82.68 inch – x
A
1,950 mm / 76.77 inch – x
1,800 mm / 70.87 inch – x
1,650 mm / 64.96 inch – x
1,500 mm / 59.06 inch – x
1,350 mm / 53.15 inch – x
1,200 mm / 47.24 inch x x
1,050 mm / 41.34 inch x x
900 mm / 35.43 inch x x
750 mm / 29.53 inch x x
The following boom lengths can be mounted on the wall bearing:

750 mm / 29.53 inch x –
A
The following boom lengths can be mounted on the

Pendant Adapter:
1,200 mm / 47.24 inch x *1 –
A
1,050 mm / 41.34 inch x –
900 mm / 35.43 inch x –
750 mm / 29.53 inch x –
*1 only on the upper boom
The following spring arms can be mounted on the booms:

– L21, 9P Springarm
– LCH19, 9P Springarm
– MD21+, WS Springarm
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Description
The following optional components can be mounted on the spring

arms:
Spring arm optional component

L21, 9P Springarm Camera bracket:
– TruVidia Camera Yoke
LCH19, 9P Springarm Camera bracket:
– TruVidia Camera Yoke
MD21+, WS Springarm Adapter:
MD26+, WS Springarm – VidiaPort Adapter VESA 100
MD40+, WS Springarm Monitor mount:
– VidiaPort Monitor Holder Single
– VidiaPort Monitor Holder Duo
MD26+, WS Springarm Adapter:
– Cable port handle
The following Trumpf Medizin Systeme products can be combined

with the spring arms:
Spring arm optional component

MD40+, WS Springarm FCS 300 Electro Cube (supply unit)
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Description
4.7 Components
4.7.1 Adapter
VidiaPort Adapter VESA 100

B
Adapter for attaching a VESA 100x100 or VESA 75x75 compatible
flat screen or other device. Horizontally rotatable (360°) and
vertically swivelling (30° downwards) monitor mount with
VESA 100/VESA 75 interface [A], extension [B] for vertical
alignment of flat screen monitors plus monitor adjustment frame
A handle [C].
The tilting function of the tilt function, and the stability of the
adjusted screen position depends on the braking force on the joint
of the monitor mount.
C
Cable port handle

As part of Philips Azurion integration, the adapter is used to mount
a maximum of 4 cables guided by the system. A strain relief
reduces the movement of the cables in the system. The adapter is
used to position the cables in accordance with the application.
4.7.2 Camera bracket
The camera bracket is used to mount a separate

TruVidia HD camera on the VidiaPort support arm system. The
TruVidia HD camera is locked onto the baseplate of the camera
mount with a bayonet lock.
A camera or handle adapter must always be attached to the mount
to compensate for the weight on the camera bracket and to cover
the electrical connections.
The difficult and easy movement of the adjustment of the
TruVidia HD camera, as well as the stability of the adjusted camera
position depends on the brake force on the brake shaft of the
TruVidia camera bracket.
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Description
4.7.3 Monitor mount
VidiaPort Monitor Holder Single

Monitor mount with horizontally rotatable and vertically swivelling
retaining bracket with VESA 100 interface [B] for flat-screen
monitors of max. 32” plus handle adapter [C] for the sterile
monitor adjustment handle.
The VidiaPort Monitor Holder Box [A] is for accommodating and
B covering the power supply unit of the flat screen.
The tilting function of the tilt function, and the stability of the
A adjusted screen position depends on the braking force on the joint
VidiaPort Monitor Holder Duo

A
Dual monitor mount with horizontally rotatable retaining bracket
and two vertically swivelling monitor mounts with VESA 100
A B
interface [B] for flat-screen monitors of max. 32” each plus two
handle adapters [C] for sterile monitor adjustment handles.
The VidiaPort Monitor Holder Boxes [A] are for accommodating
and covering the power supply unit of the flat screen.
B
C The tilting function of the tilt function, and the stability of the
adjusted screen position depends on the braking force on the joint
4.7.4 Handle adapter
The handle adapter Adaption disposable handle [A] is used to hold

adapters (products from third-party manufacturers) to which
C sterile disposable handles are attached.
The handle adapter Adaption Standard Handle [B] is used to attach
the Sterilisable Central Handle [C].
The handle adapter Adaption disposable handle [A] and Adaption
standard handle [B] can be used on the camera bracket to
compensate for the weight, as a cover for electrical connections
and to act as a guide for a sterilisable handle [C].
B If the TruVidia HD camera is disconnected from a VidiaPort
A support arm system with camera bracket, the handle adapter
Adaption disposable handle [A] or Adaption Standard handle [B]
must be attached to the camera bracket mount.
Using the handle adapter [A] or [B] on the mount of the camera
bracket and the sterile handle attached, the components can be
aligned in a sterile manner.
The handle adapter may only be used with a sterilisable or sterile
handle.
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Description
4.8 Working range

The working range is determined by the support arm system. The
support arms can be placed in any position within the operating
ranges. The spring force of the spring arms keeps the terminal
devices securely at their set height.
The hinge joints of the support arm system have been equipped
with a friction brake. The friction brake acts through the friction
force of the brake screw on the pivot pin of the support arm
component. If the boom, the spring arm, the flat screen or the
camera do not remain stable in the set swivel position, or can only
be moved with difficulty, the braking force must be adjusted by
staff trained for this work by Trumpf Medizin Systeme.
If the brake force of several support arm components needs to be
adjusted, adhere to the following sequence:
B A
1. Brake screw [A] for the boom brake
2. Brake screw [B] for the brake of the spring arm
3. Brake screw [C] for the optional brake of the monitor mount
4. Brake screw [D] for the brake of the tilt function of the
C monitor mount
The weight of the support arm component is compensated for by

a spring in the spring arm. If the spring arm does not remain steadi
in the selected height position, the spring force must be adjusted
by staff trained in this work by Trumpf Medizin Systeme. If the
spring arm rises, then the spring force is too high. If the spring arm
falls, the spring force is too low.
The swivel range of the spring arm upwards and downwards can
be individually adjusted by staff trained in this work by
Trumpf Medizin Systeme. The swivel range can be restricted until
level with the horizontal plane.
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Use
5 Use
5.1 Safety instructions

When operating devices involved in the operation, always keep
visual contact with the operation situation.
Electrical hazards:
Risk of electric shock
• No BF or CF type application components in accordance with
EN 60601-1 may be directly connected to the support arm
system.
• Do not place any objects in the device openings.
• Disconnect the support arm system from the power supply
prior to cleaning and service work.
Risk of charge balancing

• To avoid an electrostatic discharge between metallic parts of
the device and patient, the user may not touch parts of the
surgical light and the patient at the same time.
Support arm system:

Danger due to overloading
Overloading the support arm system can result in considerable
loss of function and the support arms, individual components or
accessories may come loose from their attachment and crash.
• The maximum load-bearing capacities specified in the
technical data must not be exceeded.
• Only components and accessories authorised by
Trumpf Medizin Systeme may be used on the support arm
system.
Danger due to uncontrolled movement on the support arm

system
• Before MRI use, swivel the support arms, components and
accessories from the danger area of the strong magnetic field.
• If the spring arm moves upwards or downwards of its own
accord, the spring force must be readjusted by trained
personnel.
• If the monitor mount does not remain securely in the set
position after a turning movement, the brake force must be
readjusted by trained personnel.
Risk of spring arm bouncing up

Due to a sudden reduction of weight, the spring arm may bounce
up and cause serious injuries.
• Flat screen monitors or other components must only be
mounted and removed from the spring arm by the Technical
Customer Service.
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Use
Contamination and infection:

Risk of infection for the patient
• Before first use, products must be cleaned and disinfected
according to the medical facility’s hygiene regulations.
Cleaning and disinfection are carried out by specialist
personnel trained in this area, using the cleaning and
disinfection agents approved by Trumpf Medizin Systeme.
• The sterile handle, handle adapter or the camera must not be
removed during operation.
• After each operation, the support arm system must be cleaned
and disinfected.
• Cleaning or servicing work may not be carried out during
operation.
5.2 Inspections during operation
WARNING
Risk of contamination and infection
Loose or damaged parts may fall into the wound of the patient.
• Check the support arm system for loose parts, visible damage,
in particular on the sterilisable handles.
• Check that the accessories are securely fastened to the
support arm system.
Before and after each use, the user must carry out a functional
test and visual inspection of the support arm system.
Defective or damaged devices, functional units or accessories
must be immediately taken out of operation, must be clearly
marked as defective and secured against reuse. Inform the
Technical Customer Service in the event of damage or faults.
Following any damage reported by a user, a functional check and
a visual inspection must be carried out by personnel trained to
perform these tasks by Trumpf Medizin Systeme.
Weekly inspection At least once a week, a functional check and a visual inspection
must be carried out by personnel trained to perform these tasks
by Trumpf Medizin Systeme.
Inform the Technical Customer Service in the event of damage or
faults.
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Use
Annual inspection The annual inspection must be performed by staff trained in this
work by Trumpf Medizin Systeme.
The annual inspection includes a visual inspection and function
test of the entire support arm system based on the following test
points:
– The components of the VidiaPort support arm system must be
checked for deformation
– Surface damage
– Check support arm system for damaged paintwork
– Plastic components must be checked for cracks, brittleness
and discolouration
– Welding points must be checked for cracks
– The support arm system must be checked for the
completeness of all plastic parts (such as covers and plugs)
– The device labels and signs must be checked for legibility
– The hinge joints must be checked for functionality
– The position stops must be checked for proper alignment
– Check the effect of the spring and brake forces
5.3 Connecting the power supply

The power supply must be connected by specialist staff with the
necessary access rights, knowledge and documentation
regarding the institution’s power supply.
5.4 Disconnecting the power supply

The power supply must be disconnected by specialist staff with
the necessary access rights, knowledge and documentation
regarding the institution’s power supply.
1. Switch off the terminal devices at the support arms.

2. Disconnect the support arm system from all power supply
terminals and secure it against being switched back on.
The protective earth conductor (PE) must not be
disconnected.
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Use
5.5 Attaching the handle adapter
A 1. Push the lock of the bayonet catch [A] down to position [B] so
that the three locking bores [C] of the base plate become
F accessible.
B E
G 2. Adjust the handle adapter [10] in such a way that the
D
arrangement of the three bayonet pins [D] and the two
centring pins [E] of the mount [F] at the camera bracket is
aligned with that of the locking bores [C] in the base frame
10 (this means that the alignment of the camera connectors is
also correct).
3. Press the handle adapter [10] onto the mount [F] at the
camera bracket.
4. To lock it in place, push the locking mechanism of the
bayonet catch [A] upwards so that both red markings [G] are
C aligned.
5. NOTICE! Check that the handle adapter is securely fitted on
the mount. After locking the bayonet catch, it is essential to
check that the handle adapter is securely fitted on the
mount!
H
6. Push the cover (metal ring) [H] onto the handle adapter [10]
F and the mount of the camera bracket. Ensure that the plastic
catch [I] of the mount [F] has correctly engaged in the
securing bore [K] of the cover [H].
I
K
10
5.6 Remove the handle adapter
CAUTION
Risk of short circuit
Liquid on the camera bracket can cause a short circuit and the
power supply to the mount may be interrupted.
• The camera mount must always be covered by a camera or a
handle adapter.
1. Remove the sterilisable handle from the handle adapter [10].

2. Push in the plastic latch [A] at the mount [B] and pull off the
E D
cover [C] from the handle adapter [10].
3. Hold the camera bracket in place.
B 4. Push the bayonet catch [D] down to position [E] so that the
three locking bores of the base plate become accessible.
A 5. Pull the handle adapter [10] off the mount [B] on the camera
adapter.
10
C
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Use
5.7 Positioning the component on the spring arm

To prevent damage to the product, observe the following when
positioning the components:
– When adjusting the product, take care not to collide with the
stops. Perform the setting slowly.
– Avoid collisions with other components.
– Depending on the variant, the swivel range and the vertical stop
end at the internal end stops of the boom, spring arm and the
adaptation.
– Remove any possible collision hazards before swivelling or
height adjustment.
However, if there is still a collision with other devices, wall or
ceiling, the product may be damaged and fail. After a collision,
check the product immediately for possible damage and contact
the operator if necessary.
Take hold of the component by the sterile handle [8] and move it
to the desired position.
8 8
5.8 Adjusting the braking force at the boom and spring arm
The brake force may only be adjusted by staff trained in this work
5.8.1 C-boom
There are 2 opposing brake screws on each boom.

1. Switch off the terminal devices and disconnect the support
arm system from the power supply (see Chapter 5.4).
2. Remove the left back cover [A] from the boom [4].
a) Turn the boom so that the upper PT screw [B] is
B accessible.
4
For better access to the PT screw, remove the rear cover
of the boom above it.
D
b) Using a Torx T10 screwdriver, remove the upper and lower
C PT screw [B] on the left back cover.
c) Insert a suitable slot screwdriver into the mounting
A E opening [C] of the left rear cover.
B d) Press the slot screwdriver slightly upwards and unlock the
cover.
e) Insert the slot screwdriver into the mounting opening [D]
of the right back cover [E].
f) Press the slot screwdriver slightly downwards and unlock
the cover.
g) Carefully unfold the left back cover at the edge of the two
cover panels as far as possible and remove them from the
boom.
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Use
F 3. Remove the right back cover [A] from the boom [4].
4 a) Using a Torx T10 screwdriver, remove the upper and lower
PT screw [F] on the right back cover.
b) Remove the right back cover from the boom.
F
E
4. To adjust the brake force, alternate with the same number of

rotations on both opposite brake screws [G] with a Size 5
Allen key.
G – Increase brake force:
Turn the Allen key clockwise.
4 – Reducing the brake force:
Turn the Allen key in an anticlockwise direction.
5. Test the brake force. The support arm component must be
easily adjustable and remain steady in the set swivel position.
H 6. Install the right back cover [E] on the boom [4].
F a) Position the right back cover on the boom so that the
4 upper cover [H] is inside the rear cover.
b) Attach the right back cover at the top and bottom to the
boom with a PT screw [F] (Torx T10 screwdriver).
F
E
7. Install the left back cover [A] on the boom [4].

a) Turn the boom so that the hole for the upper PT screw [B]
B is accessible.
4
b) On the connecting edge between the two rear cover
panels [A] and [E], insert the left cover into the catches [I]
of the right cover and close like a hinge.
c) Attach the left back cover at the top and bottom to the
I
boom with a PT screw [B] (Torx T10 screwdriver).
A E 8. If necessary, install the rear cover of the boom above it.
B 9. Check the firm fit of the rear cover on the boom.
– The covers on the boom must be connected to one another
with the least possible gap.
– The PT screws must be completely screwed in and may not
protrude from the cover.
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Use
5.8.2 S-boom

2. Remove the left back cover [A] from the boom [4].
a) Turn the boom so that the upper PT screw [B] is
accessible.
D B For better access to the PT screw, remove the rear cover
4 of the boom above it.
E
b) Using a Torx T10 screwdriver, remove the upper and lower
PT screw [B] on the left back cover.
C B c) Insert a suitable slot screwdriver into the mounting
F
opening [C] of the left rear cover.
d) Press the slot screwdriver slightly upwards and unlock the
A cover.
e) Insert the slot screwdriver into the mounting opening [D]
of the right back cover [E].
f) Press the slot screwdriver slightly downwards and unlock
the cover.
g) Carefully unlock the catches [F] of the left back panel at
the connecting edge between the two cover panels.
h) Remove the left back cover from the boom.
G 3. Remove the right back cover [A] from the boom [4].
4 a) Using a Torx T10 screwdriver, remove the upper and lower
PT screw [G] on the right back cover.
b) Remove the right back cover from the boom.
G E
4
rotations on both opposite brake screws [H] with a Size 5
Allen key.
H
– Increase brake force:
– Reducing the brake force:
I 6. Install the right back cover [E] on the boom [4].
G a) Position the right back cover on the boom so that the
4
upper cover [I] is inside the rear cover.
b) Attach the right back cover at the top and bottom to the
boom with a PT screw [G] (Torx T10 screwdriver).
G E
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7. Install the left back cover [A] on the boom [4].

a) Turn the boom so that the hole for the upper PT screw [B]
is accessible.
B b) At the connecting edge, insert the two rear cover panels
4 [A] and [E] and the catches [F] of the left cover at an angle
E
of 90 degrees into the catches of the right cover.
c) Close the left rear cover like a hinge.
B d) Attach the left back cover at the top and bottom to the
boom with a PT screw [B] (Torx T10 screwdriver).
F
8. If necessary, install the rear cover of the boom above it.
A 9. Check the firm fit of the rear cover on the boom.
– The PT screws must be completely screwed in and may not
5.8.3 Spring arm

2. Remove the decor caps [A] of the socket cover [B].
a) Lightly press in the right and left securing caps near the
B lugs [C] and pull the decor caps out of the openings [D].
b) Carefully open the locks [E] of the decor caps.
E A
c) Guide the right and left decor cap out of the mounts [F]
and remove.
A
F
D
4
C
3. Remove the socket cover [B] from the boom [4].
B
a) Using a Torx T10 screwdriver, remove 2 MLF screws and
H I their washers [G] from each of the right and left socket
G covers.
G
b) Carefully open the locks [H] of the socket covers.
I c) Remove the right and left socket cover together with the
B optional faceplates [I] from the boom.
4
rotations on both opposite brake screws [J] with a Size 5 Allen
J 4
key.
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6. Mount the socket cover [B] on the boom [4].

B
a) Fasten the right socket cover together with the optional
H I faceplate [I] with 2 MLF screws and washers [G] (Torx T10
Nm
G
torque screwdriver with a torque of 0.5 Nm / 0.37 ft lb) on
G the boom.
Nm
I b) Position the left socket cover together with the optional

B faceplate [I] on the right socket cover so that all locks [H]
4 are pushed together and engage.
c) Fasten the left socket cover with 2 MLF screws and
washers [G] (Torx T10 torque screwdriver with a torque of
0.5 Nm / 0.37 ft lb) on the boom.
7. Check the secure fit of the socket cover with the optional
faceplates on the boom.
– Each socket cover must be attached with 2 MLF screws and
washers.
B 8. Install the decor caps [A] of the socket cover [B].
K
a) Insert the right and left decor cap flush with the socket
E A
cover into the mounts [F], using light pressure.
b) Push the lugs [C] of the decor caps into the recesses [D] of
the socket cover and the locking mechanisms [E] into the
mounts [K] until they engage.
F 9. Check the firm fit of the decor caps in the socket cover on
A
D the boom.
4 – The decor caps must be connected to the socket cover
C with the least possible gap.
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5.9 Adjusting the spring force on the spring arm

The spring force may only be adjusted by staff trained to do so by
Trumpf Medizin Systeme.
During adjustment work, make sure that possible electrical cables
in the spring arm are routed in the centre of the spring arm and do
not slip underneath other components.
7 1. Switch off the terminal devices and disconnect the support

2. Open the lower faceplate [A].
a) Insert a suitable slot screwdriver into the opening [B].
C
b) Slightly press the slot-head screwdriver upwards and
guide the locking hooks [C] out of the rear spring arm
cover.
B
A c) Push the faceplate back into the side cover with the slot
screwdriver.
3. Swivel the spring arm [7] 5 to 10 degrees upwards.
The adjustment screw of the spring arm is relieved.
4. Carefully move any electrical cables [D] to the side and insert
an Allen key [E] Size 5 into the adjustment opening [F].
With the spring arms MD26+ and MD40+, a cable tie at the
F D electrical lines enables access to the adjustment opening.
Note the installation position of the cable tie. If necessary,
slide the cable tie to the side or remove it completely.
5. Adjust the spring force.
E – If the spring arm drops, increase the spring force:
– If the spring arm rises, decrease the spring force:
With the spring arms MD26+ and MD40+ the adjustment of
the adjustment screw can be stiff.
6. Test the spring force. The spring arm must remain steadily in
the set height position.
7 7. With the spring arms MD26+ and MD40+, restore the original
position of any cable tie previously removed at the electrical
cabling.
J – The cable tie [G] must be positioned behind the hinge lug
H [H], with the cable tie projection [I] on the right or left side
of the rear hinge.
G
– The cables [J] within the cable tie [G] must be loose.
I J
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8. Close the lower faceplate [A].

A a) Manually pull the faceplate out of the side cover and insert
C the 2 catches [K] into the rear spring arm cover.
b) Insert the slot screwdriver into the opening [B], slightly
B K press the faceplate upwards and guide the locking hooks
[C] into the rear spring arm cover.
9. Move the spring arm upwards and downwards. Check the
secure fit of the upper and lower faceplate.
– The locking hooks must sit in the rear spring arm cover.
– The plates must slide easily into the lateral guides.
5.10 Adjusting the swivel range of the control arm upwards and downwards
The swivel range may only be adjusted by staff trained in this work
Adjust the swivel range in such a way that collisions with the ceiling
or adjoining objects are avoided.
During adjustment work, make sure that possible electrical cables
in the spring arm are routed in the centre of the spring arm and do
not slip underneath other components.
5.10.1 Spring arm L21, MD21+, MD26+, MD40+

2. Pull down the spring arm [7] to relieve the adjusting screw.
C
3. Remove the front cover [A] from the spring arm [7].
B a) Press and remove the PUSH-button [B] from the right and
left front spring arm cover respectively.
A
b) Using a Torx T10 screwdriver, remove 1 MLF screw and its
washer [C] from each of the right and left front spring arm
covers.
c) Carefully unlock all catches on the connecting edge of the
7 two cover panels.
D d) Remove the front spring arm covers from the spring arm.
4. Manually push the upper and lower faceplates [D] into the
side cover of the spring arm.
5. Insert a Size 5 Allen key [E] into the adjustment opening [F].
E 6. Adjust the swivel range.
F
– Reducing the swivel range:
– Increasing the swivel range:
7. Test the swivel range.
G H F
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8. Mount the front cover [A] on the spring arm [7].

a) Rotate the recess of the segment lock [G] over the
B optional brake screw or the brake screws opening [H].
b) Position the right and left front spring arm covers on the
A
C spring arm so that, at the connecting edge between the
J two front cover panels, all catches slide into one another
Nm
and engage.
I c) Fasten the right and left spring arm cover with 1 MLF screw
7 and its washer [C] (Torx T10 torque screwdriver with a
D
torque of 1 Nm / 0.73 ft lb) each on the boom.
d) Insert 1 PUSH-button [B] flush into each of the right and
left front spring arm cover. The PUSH-button may not
9. Close the upper and lower faceplate [D].
a) Manually pull the upper and lower faceplate out of the side
cover and insert the 2 catches [I] into the front spring arm
cover.
b) Push the face plates further into the cover with a suitable
slot screwdriver, slightly press upwards and guide the
locking hooks [J] into the front spring arm cover.
– The locking hooks must fit into the front spring arm cover.
5.10.2 Spring arm LCH19

2. Pull down the spring arm [7] to relieve the adjusting screw.
C
E
B a) Press and remove the PUSH-button [B] from the left front
spring arm cover.
b) Using a Torx T10 screwdriver, remove the MLF screw and
A
its washer [C] from the left front cover.
c) Carefully unlock the catches of the left front panel at the
7 connecting edge between the two cover panels.
E D d) Remove the left front cover from the spring arm.
E
4. Remove the right front cover [D] from the spring arm [7].
a) Using a Torx T10 screwdriver, remove 3 PT screws [E] from
the right front cover.
b) Remove the right front cover from the spring arm.
5. Insert a Size 5 Allen key [F] into the adjustment opening [G].
G 6. Adjust the swivel range.
F
– Reducing the swivel range:
– Increasing the swivel range:
7. Test the swivel range.
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8. Mount the front cover on the spring arm [7].

a) Position the right front cover [D] on the spring arm so that
D
there is a gap [I] between the connecting pin of the
adaptation [H] and the cover.
b) Attach the right front cover to the spring arm with 3 PT
screws [E] (Torx T10 screwdriver).
D
E
7 H
c) Position the left front cover [A] on the spring arm so that
A there is a gap [I] between the connecting pin of the
adaptation [H] and the cover and so that, at the
Nm
A connecting edge between the two front cover panels, all
C I H
catches slide into one another and engage.
d) Fasten the left front spring arm cover with 1 MLF screw
and its washer [C] (Torx T10 torque screwdriver with a
torque of 1 Nm / 0.73 ft lb) on the spring arm.
B e) Insert 1 PUSH-button [B] flush into the left front cover. The
PUSH-button may not protrude from the cover.
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5.11 Adjusting the optional brakes on the spring arm

5.11.1 Spring arm L21, MD21+, MD26+, MD40+

a) Press and remove the PUSH-button [B] from the right and
left front spring arm cover respectively.
C
b) Using a Torx T10 screwdriver, remove 1 MLF screw and its
washer [C] from each of the right and left front spring arm
B
covers.
c) Carefully unlock all catches on the connecting edge of the
A
two cover panels.
d) Remove the front spring arm covers from the spring arm.
3. Manually push the upper and lower faceplates [D] into the
7 side cover of the spring arm.
D
4. Adjust the brake [F] with a suitable slotted screwdriver.
Turn the slotted screwdriver clockwise.
Turn the slotted screwdriver in an anticlockwise direction.
G
F
6. Mount the front cover [A] on the spring arm [7].

a) Rotate the recess of the segment lock [G] over the
B optional brake screw.
b) Position the right and left front spring arm covers on the
A
C spring arm so that, at the connecting edge between the
I two front cover panels, all catches slide into one another
Nm
and engage.
H c) Fasten the right and left spring arm cover with 1 MLF screw
7 and its washer [C] (Torx T10 torque screwdriver with a
D
torque of 1 Nm / 0.73 ft lb) each on the boom.
d) Insert 1 PUSH-button [B] flush into each of the right and
left front spring arm cover. The PUSH-button may not
7. Close the upper and lower faceplate [D].
a) Manually pull the upper and lower faceplates forwards out
of the side cover and insert the 2 catches [H] into the front
spring arm cover.
b) Push the face plates further into the cover with a suitable
slotted screwdriver, slightly press upwards and guide the
locking hooks [I] into the front spring arm cover.
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– The locking hooks must fit into the front spring arm cover.
5.11.2 Spring arm LCH19

a) Press and remove the PUSH-button [B] from the left front
spring arm cover.
C
b) Using a Torx T10 screwdriver, remove the MLF screw and
E
B its washer [C] from the left front cover.
c) Carefully unlock the catches of the left front panel at the
connecting edge between the two cover panels.
A
d) Remove the left front cover from the spring arm.
3. Remove the right front cover [D] from the spring arm [7].
7 a) Using a Torx T10 screwdriver, remove 3 PT screws [E] from
E D the right front cover.
E
b) Remove the right front cover from the spring arm.
4. Move the segment safety catch [F].
G F a) Using a Torx T10 screwdriver, remove 1 MLF screw [G] from
the segment fuse.
b) Push the segment lock forwards until the brake screw [H]
is accessible.
5. Adjust the brake [H] with a suitable slotted screwdriver.

Turn the slotted screwdriver clockwise.
Turn the slotted screwdriver in an anticlockwise direction.
H
7. Move the segment safety catch [F].

a) Push the segment lock backwards until it no longer
protrudes over the mounting opening [I].
b) Attach the segment lock to the spring arm using 1 MLF
screw [G] (Torx T10 screwdriver).
F
I
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8. Mount the front cover on the spring arm [7].

a) Position the right front cover [D] on the spring arm so that
G D
there is a gap [K] between the connecting pin of the
adaptation [J] and the cover.
b) Attach the right front cover to the spring arm with 3 PT
screws [E] (Torx T10 screwdriver).
D
E
7 J
c) Position the left front cover [A] on the spring arm so that
A there is a gap between the connecting pin of the
adaptation and the cover and so that, at the connecting
Nm
A edge between the two front cover panels, all catches slide
C K J
into one another and engage.
d) Fasten the left front spring arm cover with 1 MLF screw
and its washer [C] (Torx T10 torque screwdriver with a
torque of 1 Nm / 0.73 ft lb) on the spring arm.
B e) Insert 1 PUSH-button [B] flush into the left front cover. The
PUSH-button may not protrude from the cover.
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5.12 Setting the braking force on the components

5.12.1 Monitor mount
The adjustment should only be made when the flat screen monitor
A is completely mounted.
A
A
2. If necessary, remove the VidiaPort Monitor Holder Box.
rotations on both opposite screws [A], using a Size 4 Allen
key.
4. Adjust the brake force.
5. Test the brake force. The monitor bracket must be easily
adjustable and remain steady in the set position.
6. If necessary, reinstall the VidiaPort Monitor Holder Box.
5.12.2 Adapter
VidiaPort Adapter VESA 100

The adjustment should only be made when the flat screen monitor
is completely mounted.
B 2. Loosen both threaded pins [A], using a Size 3 Allen key.
B rotations on both opposite screws [B], using a Size 8 Allen
key.
A – Increase brake force:
A Turn the Allen key clockwise (with a maximum torque of
18 Nm / 13.14 ft lb).
Turn the Allen key anticlockwise (with a maximum torque of
18 Nm / 13.14 ft lb).
4. Tighten the two threaded pins [A] with a maximum torque of
4 Nm / 2.92 ft lb.
5. Test the brake force. The adapter must be easily adjustable
and remain steady in the set position.
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5.12.3 Camera bracket
Any adjustment is only permissible with the TruVidia HD camera

installed (including sterilisable handle).
2. Remove the three screws [A] using a suitable Allen key and
remove the housing cover [B].
B 3. The adjusting screw [C] for the brake is secured with a
toothed washer. Disengage the tooth [D] from the securing
groove [E] so that the adjusting screw can be freely moved.
C 4. Use a size 27 open-end spanner to set the braking force of
A the adjusting screw [C].
Turn the open-end spanner clockwise.
D
E – Reducing the brake force:
Turn the open-end spanner in an anticlockwise direction.
5. Secure the adjusting screw [C] again. To do so, bend one of
the teeth in the tooth washer back into the securing groove
[E] (if this is not possible in any other way due to the rotation
position, bend the tooth towards the setting screw).
6. Test the brake force. The camera must be easily adjustable
and remain steady in the set position.
7. Replace the housing cover [B] and fasten it in place with the
3 screws [A].
5.13 Maximum load

The various central axes, extension arm versions and boom
lengths result in different combination options of the products
and therefore differ with regard to maximum permissible load-
bearing capacities. The total capacity of the VidiaPort support arm
system is on the device label of the support arm system and must
be strictly adhered to.
The maximum load on the spring arm in a VidiaPort support arm
system depends on their booms in the support arm system, the
boom versions, boom positions and boom length.
Attention: the maximum permissible load-bearing capacity of the
spring arm may be greater than the load-bearing capacity of the
boom in the support arm system. The carrying capacity of the
support arm system must be adhered to.
The maximum load-bearing capacity of the support arm system
and spring arm and the net weights of monitor mount and
VidiaPort Monitor Holder Box are listed in Chapter 12. The tare
weights can also be identified and determined using the
Trumpf Medizin Systeme material number (REF) on the device
label.
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The calculation of the maximum additional load of a spring arm is

required for selection of the flat screen(s) used.
– The following form applies to spring arms MD21+, MD26+ and
MD40+:
Maximum additional load (weight) = maximum load-bearing
capacity on the spring arm - tare weight of the monitor mount
- tare weight of the VidiaPort monitor Holder Box(s)
Ensure that a VidiaPort Monitor Holder Box is used for each flat
screen power supply.
Example for calculation of the maximum additional load for a

spring arm in a support arm system:
In a support arm system C2S1, the monitor mount
VidiaPort Holder Duo (boom length 1,050 mm / 41.34 inch) of the
spring arm MD40+ and two VidiaPort Monitor Holders Boxes are
mounted.
Maximum load-bearing capacity of the spring arm depending on
the boom length: 40 kg / 88 lbs
Tare weight of monitor mount (with the handles below):
8 kg / 17.6 lbs
Tare weight of the VidiaPort Monitor Holder Box: 1 kg / 2.2 lbs
Maximum additional load: 40 kg - 8 kg - 1 kg - 1 kg = 30 kg /
88 lbs - 17.6 lbs - 2.2 lbs - 2.2 lbs = 66 lbs
5.14 Decommissioning
WARNING
Danger of infection
The product may be contaminated with infectious substances.
• The product must always be disinfected before temporarily or
permanently taking out of service.
For temporary or permanent decommissioning, disconnect the

VidiaPort support arm system from all power supply terminals (see
Chapter 5.4) and secure it against being switched back on, then
clearly mark it as being out of order. Permanent decommissioning
of the VidiaPort support arm system may only be carried out by a
qualified service technician.
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Cleaning and disinfection
6 Cleaning and disinfection

For safe use of the VidiaPort support arm system, it must be
cleaned and disinfected at regular intervals after each operation,
using suitable cleaners and disinfectants.
WARNING
Risk of infection for the patient
• No cleaning work may be carried out during operation.
WARNING
Incorrectly used cleaners or disinfectants can endanger
patients or cause damage to products.
If the specifications and instructions contained in this chapter are
not observed or complied with, this may result in a risk of
contamination or infection for the patient or damage to the
product. Furthermore, it would render any warranty claim void.
• Dose cleaners and disinfectants in such a way that no liquid can
enter into gaps or openings of the VidiaPort support arm
system.
• Use surface disinfectants only in the concentration specified
by the manufacturer.
• Only use disinfectants approved by the manufacturer for use
with the following materials:
Polycarbonate (PC), polyamide (PA), acrylonitrile butadiene
styrene copolymer (ABS), polystyrene (PS), polyurethane (PUR),
polyphenylene sulphide (PPSU), polyvinylchloride (PVC),
polybutylene terephthalate (PBT) and silicones.
• In the event of an excessive coating of surface disinfectant
forming, carry out thorough cleaning.
Due to the risk of surface damage, the following need to be taken
into account:
• Do not use sharp, pointed or abrasive objects.
• Do not use abrasive substances or agents which can remove
material.
• Do not use solvents, benzene, paint thinners, alkaline cleaning
agents or cleaning agents containing acid or aldehyde.
• Do not use agents with glycol derivatives, phenols, phenol
derivatives or quaternary compounds.
• To prevent paint or corrosion damage, only use agents that do
not contain chlorides or halogenides.
• It is essential that the hygiene instructions of the operator are
observed.
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NOTICE
Weight balancing
• If the TruVidia HD camera is disconnected from a VidiaPort
support arm system with TruVidia HD camera frame, the handle
adapter # 2065945 (Adaption Standard handle) must be
attached as a counterweight and as a guide for the sterilisable
handle. The sterilisable handle cannot be attached without the
handle adapter (Adaption Standard handle).
For cleaning and disinfection of all components and products -

including those from other manufacturers - always read and
comply with the instructions for use.
Adhere to national regulations:

The operator must observe the requirements of the responsible
national hygiene and disinfection board.
6.1 Recommended disinfectants

Trumpf Medizin Systeme recommends the following disinfectants
for manual application:
Manufacturer Designation
B. Braun Melsungen AG Meliseptol
Various 70 % 2-propanol alcohol
Schülke & Mayr GmbH Perform 0.5 %
Bode Chemie GmbH & Co. KG Dismozon pure 0.75 %
Clorox Healthcare Hydrogen Peroxide Cleaner
Disinfectant Wipes
Kesla Pharma Wofasteril 0.5 %
The hygiene guidelines of the product and the instructions of the

disinfectant manufacturer must be taken into account.
The information on the disinfectants, regarding application
concentrations and exposure time, must be followed.
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The following disinfectants are permitted to disinfect the surfaces

of the support arm system (ceiling pipe, central axis, boom and
spring arms):
Preparation Ingredient
Meliseptol Alcohols/aldehydes
Ethanol 60 % Alcohols
Chlorhexidine 0.5 % in 70 % Chlorine-based
ethanol
Chlorine 250 ppm in 1 litre of Chlorine-based
distilled water
Haemosol 1 % in 1 litre of water Guanidine derivative
Dismozon pure Peroxide compounds
Incidin Extra N Quaternary compound,
alkylamine derivative
Terralin protect Quaternary compound, glycol
derivative
6.2 Preparation
WARNING
Risk of electric shock
Touching live components may result in electric shock.
• Prior to cleaning and disinfection, disconnect the VidiaPort
support arm system from all power supply terminals.
• Do not place any objects in the device openings.
1. Disconnect the VidiaPort support arm system from the power

supply and secure it against being switched back on. See
Chapter 5.4.
2. If necessary, remove the TruVidia HD camera. The handle
adapter #2065945 (Adaption Standard handle) or #2066135
(Adaption disposable handle) must be attached to the
camera bracket as a compensation weight.
If the VidiaPort support arm system with its attached camera
bracket and TruVidia HD camera is switched off while the control
system is still in operation, the control program will detect an error
due to the control system not being able to communicate with the
camera.
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6.3 Cleaning and disinfection of the VidiaPort support arm system

Warranty claim: Failure to comply with cleaning or disinfection
requirements will render any warranty claim void. No warranty is
accepted for damage which is due to the use of unsuitable
cleaning agents or disinfectants. The warranty applies only to
undamaged surfaces.
Cleaning and disinfection of the VidiaPort support arm system
may only be carried out by a hygiene professional or a person
suitably trained by a hygiene professional.
Cleaning and disinfection may only be carried out using agents
and chemicals that have been tested and approved in regard to
their material compatibility by Trumpf Medizin Systeme, see
Chapter 6.1. If an agent is not included on the list, it should not be
used as otherwise functional components could be changed or
damaged.
Thorough cleaning of visible contamination, for example from
body fluids, must be carried out before actual disinfection.
– It is not permissible to use sharp, pointy or abrasive objects nor
any abrasive agents or means that cause material removal for
cleaning since this could cause damage to surfaces.
– Damaged surfaces can be penetrated and destroyed by
chemical substances.
– Only soft brushes and mild cleaners or cleaning disinfectants
may be used to remove strong and persistent dirt. Disinfection
may only start after no more visible dirt can be found.
– During cleaning and disinfection, do not insert any objects into
the device openings.
After a risk of contamination of the product through potentially
infectious material (e.g. blood, secretions or excrements),
disinfect the surfaces immediately.
Use the wipe-over method only for disinfection. Disinfection by
UV irradiation or steaming is not permitted.
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6.3.1 Wipe disinfection
DANGER
Risk of fire or explosion due to disinfectants
Formation of gases, fumes or mists when using disinfectants may
create a combustible or explosive atmosphere.
• Do not use highly flammable disinfectants.
• Do not disinfect large areas.
• Allow hot surfaces to cool down before disinfection.
• Where possible, completely isolate the room’s electrical
systems or ensure that no switching – especially automatic
switching – is initiated or takes place whilst disinfection is in
progress.
• After wipe-over disinfection, wait until the disinfectant has
dried completely.
• Ensure that the room is adequately ventilated.
Wipe-over disinfection is used to disinfect the VidiaPort support

arm system.
For cleaning and disinfection, wipe the device components with a
damp but not wet cloth. Wiping should apply only a thin film of
liquid and after wiping only a thin coherent film of moisture should
remain. From the microbiological point of view, this moisture film
is entirely sufficient. Liquid should not pool on the surface.
If too much liquid is applied to the surface during disinfection,
residue will be left on the product. These may lead to faulty
measurements, particularly through the cover pane of the sensor.
To prevent the build-up of a coating of disinfectant residues,
regular cleaning with a mild all-purpose cleaner is necessary.
The regularity of cleaning will depend on the frequency of
disinfection but must be at least once a month.
Cleaning procedure
1. Disconnect the VidiaPort support arm system from all power
supply terminals and secure it against being switched back
on.
2. Allow the device components to cool. Only clean/disinfect
the VidiaPort support arm system when it is cold.
3. Moisten a cloth with some cleaning or disinfecting agent.
4. Only wipe the VidiaPort support arm system using a damp
(not wet) cloth.
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Troubleshooting
7 Troubleshooting
If a fault recurs or cannot be remedied, put the device out of service and contact Trumpf Medizin
Systeme Technical Customer Service.
Error Cause Fix

Attached accessory drops / rises Spring force in spring arm is too Have the spring force adjusted
weak / too strong. by staff trained in this work by
Attached accessory is tensed / Brakes set too stiff/loose. Have the brakes adjusted by staff
loosened trained in this work by
8 Maintenance
WARNING
Do not perform servicing work during surgery or while in
operation.
The VidiaPort support arm system must be maintained at least

every 2 years after handover to the user: After ten years of
operation, maintenance of the support arm system must be
carried out annually.
Only qualified service technicians may perform maintenance on
the products or replacement of components.
The contact details for service technicians are available from the
Technical Customer Service of Trumpf Medizin Systeme.
Trumpf Medizin Systeme recommends that a maintenance
agreement be concluded so that maintenance can be performed
reliably and in time.
7990089_002_01 – 2079217 – 2021-11-12 53

Repair
9 Repair
WARNING
Do not perform servicing work during surgery or while in
operation.
Only qualified service technicians may repair the products. The

contact details for service technicians are available from the
Technical Customer Service of Trumpf Medizin Systeme.
After each repair, an electrical safety inspection according to the
criteria specified by Trumpf Medizin Systeme must be carried out.
10 Spare parts
The wearing parts may only be exchanged by staff trained in this
work by Trumpf Medizin Systeme.
number
Wearing parts on the boom
SP-ValiaS, breaking screws M10 1946894
Wearing parts on the spring arm
SP-VALiA, Springarms Basic, brakescrews M10 1946909
54 7990089_002_01 – 2079217 – 2021-11-12

Disposal
11 Disposal
Within the European Union, the product is governed by Directive
2012/19/EU on waste electrical and electronic equipment and
complies with the requirements of Directive 2011/65/EU of the
European Parliament and of the Council of 8 June 2011 on the
restriction of the use of certain hazardous substances in electrical
and electronic equipment, as amended by Commission Delegated
Directive (EU) 2015/863 of 31 March 2015 as regards the list of
restricted substances (RoHS). The support arm system must not
be disposed of via the communal collection points for old
electrical equipment.
In countries outside the European Union (EU), the legal
requirements of the respective country must be observed.
Please contact the Trumpf Medizin Systeme Technical Customer
Service, the local sales representative or the appropriate national
authority if you have any questions about proper disposal.
In addition to regional disposal, faulty products or products that
are no longer used may be returned to Trumpf Medizin Systeme.
Trumpf Medizin Systeme then takes responsibility for
environmentally friendly disposal. Detailed information on returns
is available from the Trumpf Medizin Systeme Technical Customer
Service.
7990089_002_01 – 2079217 – 2021-11-12 55

Technical data
12 Technical data
12.1 Device data
IP classification according to IEC 60529

Support arm system IP30
Monitor mount IP10
Mode of operation
Support arm system Continuous operation
Own weight
Designation Material Weight
number
Spring arm
L21, 9P Springarm 2077411 7.3 kg / 16.1 lbs
LCH19, 9P Springarm 2077413 6.7 kg / 14.8 lbs
MD21+, WS Springarm 2077407 7.8 kg / 17.2 lbs
Adapter
VidiaPort Adapter VESA 100 2077992 3 kg / 6.6 lbs
Cable port handle 2082139 14.3 kg / 31.5 lbs
Monitor mount
VidiaPort Monitor Holder Single 2078861 handle below
approx. 5 kg / 11.1 lbs
handle on the side
approx. 5.5 kg / 12.1 lbs
(without VidiaPort monitor Holder
Box, including sterilisable handle)
VidiaPort Monitor Holder Duo 2078862 handle below
handle on the side
(without VidiaPort monitor Holder
Boxes, including sterilisable handles)
VidiaPort Monitor Holder Box 2078863 1 kg / 2.2 lbs
Dimensions of/monitor(s) for monitor mount

VidiaPort Monitor Holder Single maximum 32”
VidiaPort Monitor Holder Duo maximum 32”
56 7990089_002_01 – 2079217 – 2021-11-12

Technical data
Spring arm L21, 9P Springarm
A
Spring arm length 920 mm / 36.22 inch
[A]
B
Tilting range horizontal [B] 360°
vertical [C] +45° to -70°
C Cable passage Maximum 2x 9 mm / 2x 0.35 inch
Electrical interface H9, 9-pin interface for a camera
Spring arm LCH19, 9P Springarm
Spring arm length 735 mm / 28.94 inch
A
[A]
B
vertical [C] +45° to -70° with a
C limited load capacity
+20° to -70° with
maximum capacity
Electrical interface H9, 9-pin interface for a camera
Sprint arm MD21+, WS Springarm, MD26+, WS Springarm, MD40+, WS Springarm
A Spring arm length 920 mm / 36.22 inch

[A]
B
vertical [C] +45° to -70°
C Cable passage MD21+, WS 253 mm² / 0.39 inch²
Springarm
MD26+, WS 510 mm² / 0.79 inch²
Springarm on axis with C- and
S-booms
488 mm² / 0.76 inch²
on axis, only with
S-boom
MD40+, WS 510 mm² / 0.79 inch²
Springarm
7990089_002_01 – 2079217 – 2021-11-12 57

Technical data
12.2 Load bearing capacities

12.2.1 Boom
The following information concerning the maximum load-bearing

capacity on the boom already takes the weight of the spring arm
into account.
S1 support arm system (1 S-boom on a central axis)

Material Boom length Load bearing capacity
number
2077289 750 mm / 29.53 inch 26 kg / 57 lbs
2077290 750 mm / 29.53 inch 26 kg / 57 lbs
2077291 750 mm / 29.53 inch 26 kg / 57 lbs
2077292 900 mm / 35.43 inch 26 kg / 57 lbs
2077293 900 mm / 35.43 inch 26 kg / 57 lbs
2077295 900 mm / 35.43 inch 26 kg / 57 lbs
2077294 1,050 mm / 41.34 inch 26 kg / 57 lbs
2077296 1,050 mm / 41.34 inch 26 kg / 57 lbs
2077297 1,050 mm / 41.34 inch 26 kg / 57 lbs
2077298 1,200 mm / 47.24 inch 21 kg / 46 lbs
2077299 1,200 mm / 47.24 inch 21 kg / 46 lbs
2077300 1,200 mm / 47.24 inch 21 kg / 46 lbs
C1 support arm system (1 C-boom on a central axis)

number
2077302 750 mm / 29.53 inch 40 kg / 88 lbs (only centrally)
2077301 900 mm / 35.43 inch 40 kg / 88 lbs (only centrally)
2077303 1,050 mm / 41.34 inch 40 kg / 88 lbs (only centrally)
2077311 1,650 mm / 64.96 inch 37 kg / 81 lbs
2077312 1,650 mm / 64.96 inch 37 kg / 81 lbs
2077313 1,650 mm / 64.96 inch 37 kg / 81 lbs
2077314 1,800 mm / 70.87 inch 34 kg / 74 lbs
2077316 1,800 mm / 70.87 inch 34 kg / 74 lbs
2077317 1,800 mm / 70.87 inch 34 kg / 74 lbs
2077315 1,950 mm / 76.77 inch 31 kg / 68 lbs
2077318 1,950 mm / 76.77 inch 31 kg / 68 lbs
2077320 1,950 mm / 76.77 inch 31 kg / 68 lbs
58 7990089_002_01 – 2079217 – 2021-11-12

Technical data

number
2077319 2,100 mm / 82.68 inch 28 kg / 61 lbs
2077321 2,100 mm / 82.68 inch 28 kg / 61 lbs
2077322 2,100 mm / 82.68 inch 28 kg / 61 lbs
2077323 2,250 mm / 88.58 inch 26 kg / 57 lbs
2077324 2,250 mm / 88.58 inch 26 kg / 57 lbs
2077325 2,250 mm / 88.58 inch 26 kg / 57 lbs

number
2077326 900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 21 kg / 46 lbs
2077327 900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 21 kg / 46 lbs
2078860 900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 21 kg / 46 lbs
2077328 900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 21 kg / 46 lbs
2077331 1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077332 1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077333 1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077334 1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077339 1,200 mm / 47.24 inch 18 kg / 39 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
2077340 1,200 mm / 47.24 inch 18 kg / 39 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
2077341 1,200 mm / 47.24 inch 18 kg / 39 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
2077342 1,200 mm / 47.24 inch 18 kg / 39 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
7990089_002_01 – 2079217 – 2021-11-12 59

Technical data

number
2078859 900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 40 kg / 88 lbs
2077338 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 40 kg / 88 lbs
2077346 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 40 kg / 88 lbs
2077352 1,350 mm / 53.15 inch 40 kg / 88 lbs
1,200 mm / 47.24 inch 40 kg / 88 lbs
2077351 1,500 mm / 59.06 inch 40 kg / 88 lbs
1,350 mm / 53.15 inch 40 kg / 88 lbs
2077353 1,500 mm / 59.06 inch 40 kg / 88 lbs
1,350 mm / 53.15 inch 40 kg / 88 lbs
2077354 1,500 mm / 59.06 inch 40 kg / 88 lbs
1,350 mm / 53.15 inch 40 kg / 88 lbs
2077355 1,500 mm / 59.06 inch 40 kg / 88 lbs
1,350 mm / 53.15 inch 40 kg / 88 lbs
2077356 1,500 mm / 59.06 inch 40 kg / 88 lbs
1,350 mm / 53.15 inch 40 kg / 88 lbs
2077376 1,650 mm / 64.96 inch 37 kg / 81 lbs
1,500 mm / 59.06 inch 40 kg / 88 lbs
2077357 1,650 mm / 64.96 inch 37 kg / 81 lbs
1,500 mm / 59.06 inch 40 kg / 88 lbs
2077358 1,650 mm / 64.96 inch 37 kg / 81 lbs
1,500 mm / 59.06 inch 40 kg / 88 lbs
2077359 1,650 mm / 64.96 inch 37 kg / 81 lbs
1,500 mm / 59.06 inch 40 kg / 88 lbs
2077360 1,650 mm / 64.96 inch 37 kg / 81 lbs
1,500 mm / 59.06 inch 40 kg / 88 lbs
2077361 1,800 mm / 70.87 inch 34 kg / 74 lbs
1,650 mm / 64.96 inch 37 kg / 81 lbs
2077362 1,800 mm / 70.87 inch 34 kg / 74 lbs
1,650 mm / 64.96 inch 37 kg / 81 lbs
2077363 1,800 mm / 70.87 inch 34 kg / 74 lbs
1,650 mm / 64.96 inch 37 kg / 81 lbs
2077364 1,800 mm / 70.87 inch 34 kg / 74 lbs
1,650 mm / 64.96 inch 37 kg / 81 lbs
2077365 1,800 mm / 70.87 inch 34 kg / 74 lbs
1,650 mm / 64.96 inch 37 kg / 81 lbs
2077366 1,950 mm / 76.77 inch 31 kg / 68 lbs
1,800 mm / 70.87 inch 34 kg / 74 lbs
60 7990089_002_01 – 2079217 – 2021-11-12

Technical data

number
2077367 1,950 mm / 76.77 inch 31 kg / 68 lbs
1,800 mm / 70.87 inch 34 kg / 74 lbs
2077368 2,100 mm / 82.68 inch 28 kg / 61 lbs
1,950 mm / 76.77 inch 31 kg / 68 lbs
2077369 2,100 mm / 82.68 inch 28 kg / 61 lbs
1,950 mm / 76.77 inch 31 kg / 68 lbs
2077375 2,250 mm / 88.58 inch 26 kg / 57 lbs
2,100 mm / 82.68 inch 28 kg / 61 lbs
2077370 2,250 mm / 88.58 inch 26 kg / 57 lbs
2,100 mm / 82.68 inch 28 kg / 61 lbs
Support arm system C1S1 (1 C-boom and 1 S-boom on a central

axis)
number
2079337 900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077329 900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077330 900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077335 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 26 kg / 57 lbs
2077336 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 26 kg / 57 lbs
2077337 1050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 26 kg / 57 lbs
2077343 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077344 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077345 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077347 1,350 mm / 53.15 inch 40 kg / 88 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077348 1,350 mm / 53.15 inch 40 kg / 88 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077349 1,350 mm / 53.15 inch 40 kg / 88 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
7990089_002_01 – 2079217 – 2021-11-12 61

Technical data
Support arm system C1S1 (1 C-boom and 1 S-boom on a central

axis)
number
2077350 1,350 mm / 53.15 inch 40 kg / 88 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs

number
2077371 1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 21 kg / 46 lbs
2077372 1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 21 kg / 46 lbs
Support arm system C1S2 (1 C-boom and 2 S-booms on a

central axis)
number
2077373 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077374 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077380 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077382 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077381 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
2077383 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
62 7990089_002_01 – 2079217 – 2021-11-12

Technical data
Support arm system C2S1 (2 C-booms and 1 S-boom on a

central axis)
number
2077377 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077378 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077379 1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 40 kg / 88 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077384 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 26 kg / 57 lbs
2077385 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 26 kg / 57 lbs
2077386 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 40 kg / 88 lbs
900 mm / 35.43 inch 26 kg / 57 lbs
2077387 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077388 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077389 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077390 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077392 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077391 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
2077394 1,350 mm / 53.15 inch 35 kg / 77 lbs
1,200 mm / 47.24 inch 35 kg / 77 lbs
1,050 mm / 41.34 inch 26 kg / 57 lbs
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Technical data
Support arm system C2S1 (2 C-booms and 1 S-boom on a

central axis)
number
2077393 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077395 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077396 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077397 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077399 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077398 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
2077401 1,500 mm / 59.06 inch 31 kg / 68 lbs
1,350 mm / 53.15 inch 31 kg / 68 lbs
1,200 mm / 47.24 inch 21 kg / 46 lbs
Support arm system C2S2 (2 C-boom and 2 S-boom on a

central axis)
number
2077400 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077402 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
2077403 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
64 7990089_002_01 – 2079217 – 2021-11-12

Technical data
Support arm system C2S2 (2 C-boom and 2 S-boom on a

central axis)
number
2077404 1,200 mm / 47.24 inch 40 kg / 88 lbs
1,050 mm / 41.34 inch 21 kg / 46 lbs
900 mm / 35.43 inch 21 kg / 46 lbs
750 mm / 29.53 inch 26 kg / 57 lbs
12.2.2 Spring arm
The following information on the maximum load-bearing capacity on the spring arms
MD21+, MD26+ and MD40+ complies with the tare weight of the flat screen connection, the
flat screen(s) and the VidiaPort Monitor Holder Box(s).
Designation Material Spring Load bearing capacity

number arm length
L21, 9P Springarm 2077411 920 mm / 1.5 kg to 21 kg /
36.22 inch 3.3 lbs to 46 lbs
LCH19, 9P Springarm 2077413 735 mm / 20 Nm to 200 Nm /
28.94 inch 14.6 ft lb bis 146 ft lb
MD21+, WS Springarm 2077407 920 mm / 1.5 kg to 21 kg /
36.22 inch 3.3 lbs to 46 lbs
MD26+, WS Springarm 2077408 920 mm / 13 kg to 26 kg /
36.22 inch 28 lbs to 57 lbs
MD40+, WS Springarm 2077409 920 mm / 18 kg to 40 kg /
36.22 inch 39 lbs to 88 lbs
12.3 SVHC (Substance of very high concern)

The products may contain components having constituents which
must be notified of in accordance with Article 33 of
REACH Regulation (EC) No. 1907/2006, with a concentration of
over 0.1% weight by weight. Trumpf Medizin Systeme will provide
you with the list of affected components on request. You can also
view the list online at hillrom.com.
7990089_002_01 – 2079217 – 2021-11-12 65

Product certification
13 Product certification
13.1 European Union

The support arm system is a Class I medical device according to
Regulation 2017/745/EU concerning medical devices and is
compliant with the version of the Regulation currently in force at
the time of product sale. Trumpf Medizin Systeme declares the
conformity of the support arm system with the General Safety and
Performance Requirements of Regulation 2017/745/EU
concerning medical devices, according to Annex I.
Implementation of the compliance assessment procedure
required for a Class I medical device takes place according to
Article 52, Paragraph 7, taking into account the quality
management system according to Annex IX, Chapter 1. The
manufacturer certifies conformity with the CE marking.
13.2 USA/Canada
ETL Mark: Product was tested by Intertek for USA and Canada.
ETL classification regarding risk of electric shock and fire as well as
mechanical hazard in accordance with ULSTD 60601-1;
CAN/CSA STD C22.2 NO.601.1.
13.3 Ukraine
Це маркування підтверджуЕ, що вироби, промарковані знаком
відповідності, пройшли всі необхідні процедури підтвердження
відповідності та підкоряються визначенимтехнічним керівництвам
України.
Відповідність: Технічний регламент щодо медичних виробів,
затверджений Постановою Кабінету міністрів України від 02 жовтня
2013 р. N° 753
13.4 Serbia
Certificate/Registration number: 515-02-03704-16-001
66 7990089_002_01 – 2079217 – 2021-11-12

7990089_002_01 – 2079217 – 2021-11-12

Vidia Port

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Instructions for use

Manufacturer TRUMPF Medizin Systeme GmbH + Co. KG

Authorised Australian Sponsor Trumpf Med (Aust) Pty Ltd

Information about the document Original instructions for use

7990089_002_01 – 2079217 – 2021-11-12 3

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4 7990089_002_01 – 2079217 – 2021-11-12

Signal word Meaning

© TRUMPF Medizin Systeme GmbH + Co. KG

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6 7990089_002_01 – 2079217 – 2021-11-12

7990089_002_01 – 2079217 – 2021-11-12 7

6 Cleaning and disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

12 Technical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .56

8 7990089_002_01 – 2079217 – 2021-11-12

1.1 Intended purpose

1.3 Patient definition

1.4 User definition

1.5 Use environment

Temperature: +10 °C to +40 °C / 50 °F to 104 °F

1.6 Storage and transport conditions

Temperature: -15 °C to +40 °C / 50 °F to 104 °F

Air pressure: 70 kPa to 106 kPa / 10 psi to 15 psi

7990089_002_01 – 2079217 – 2021-11-12 9

Fragile packaged goods

Protect against moisture

1.7 Service life

10 7990089_002_01 – 2079217 – 2021-11-12

Monitor mount Designation Material

2.2 Combination with other Trumpf Medizin Systeme products

7990089_002_01 – 2079217 – 2021-11-12 11

Surgical light Designation Material Document

2.3 Combination with products of other manufacturers

Designation Manufacturer Material

The support arms may be operated in combination with the

12 7990089_002_01 – 2079217 – 2021-11-12

2.4 Responsibility of the operator

7990089_002_01 – 2079217 – 2021-11-12 13

– Signs on the product inform about residual risks during use or

2.5.2 Location and meaning

No. Sign Meaning

[B] Manufacturer’s logo

[C] not available –

14 7990089_002_01 – 2079217 – 2021-11-12

No. Sign Meaning

Unique Device Identification (UDI) comprising:

Product is declared compliant with Regulation 2017/745/EU

7990089_002_01 – 2079217 – 2021-11-12 15

VidiaPort Ceiling Single/Duo/Trio

Various monitor mounts (maximum 2 flat screens on a monitor

There are 2 versions of booms:

A maximum of 4 booms (2 C-booms and 2 S-booms) can be

16 7990089_002_01 – 2079217 – 2021-11-12

4.1 VidiaPort Ceiling Single support arm system

7990089_002_01 – 2079217 – 2021-11-12 17

[1] Ceiling conduit

4.2 VidiaPort Ceiling Duo support arm system

18 7990089_002_01 – 2079217 – 2021-11-12

– two medical flat screen monitors [11] (products from third-party

[1] Ceiling conduit

7990089_002_01 – 2079217 – 2021-11-12 19

4.3 VidiaPort Ceiling Trio support arm system