Professional Documents
Culture Documents
Service Manual
Service Manual
Mach
Lamps and Engineering
MACH 130 FP
Mains voltage 230V / 120V
List of contents
1. Safety instructions ............................................................................................ Page 3
5. Cleaning............................................................................................................ Page 9
5.1 Sterilizable handle ...................................................................................... Page 9
5.2 Lamp head, protective disk......................................................................... Page 11
1. Safety instructions
Please pay attention to the directions for use when handling the lamp.
Attention:
This device is not suitable for use in hazardous locations. The lamp is classified
as a Group 1 device according to the regulations for EEMP.
Repairs to the lamp and special installation work on the reflector or plug-in socket should
only be carried out by ourselves or a company expressly authorised by ourselves.
The manufacturer is only responsible for the safety of the lamp if repairs and alterations have
been carried out by themselves or a company who can guarantee that the safety regulations
have been observed.
The manufacturer is not liable for personal or material damages if the lamp is misappropri-
ately or incorrectly operated or misused.
The lamp body may only be dismantled from the spring arm in reverse order to its assembly
after the assembly locking device has been inserted and tightened since the arm is under
spring tension.
Make sure that the lamp is in perfect working order before every use.
The lamps Mach 130 FP may not be used without the dielectric filter disk.
The dielectric filter disk between reflector and protective disk prevents a damaging heating of
the illuminated area.
2. Mounting layout
Wall attachment
Bracket
Circlip
Levelling washer (Remark!)
Levelling washer
Spring arm
OT -lamp
Remark:
One levelling washer is always necessary.
If the distance between wall bracket and spring arm is too big, use the second levelling washer.
The circlip (Seegerring) must be easy to mount and has to snap in. It should turn easily in the groove.
• Unscrew the cover 1 (with sliding contact plug) from the articulated arm.
• Slide the articulated arm from below into the upper articulated arm.
• Slide the levelling washer and safety ring onto the connection tube of the spring arm in the correct or-
der.
• Place the safety ring in position.
Ensure that the safety ring slots properly in the groove of the coupling journal (tool: mounting pliers).
• Place the cover back on the articulated arm and screw tight.
• Disconnect the electrical connection (in case of direct electrical connection using the fuses).
• Unscrew the cover 1 (with sliding contact plug) from the articulated arm.
• Pull the cover 1 off upwards by lateral compressing.
• Remove the levelling washer and safety ring with the mounting pliers and pull the suspension tube out
in a downwards movement.
Caution:
The lamp may only be dismounted (in reverse order to the mounting procedure) after the mount-
ing safeguard has been positioned and screwed tight, as the arm is under spring tension.
Lamp features:
• Mach 130 FP with focusable light field size and
integrated dielectric filter disk.
The reflector is adapted to the dielectric filter
disk.
67,68
4.2 Positioning
Use the handle or the handle rail GL to position the
GL lamp.
45
45
5. Cleaning
V 5.1 Sterilizable handle
The lamps Mach 130/Mach 130F 22,8V UL/Uniflex
R96 120V UL can be equipped as an option with a
sterilizable handle 45.
The sterilizable handle 45 is removable and steriliz-
45 able. Before using the first time and before every
use the handle sleeve must be cleaned, disinfected
and sterilised.
Basics
Efficient cleaning / disinfection is an essential requirement for effective sterilisation of the handle.
Within the scope of responsibility for the sterility of the products it should be noted that only sufficiently
validated equipment and product specific processes are used for cleaning / disinfection and that the vali-
dated parameters are complied with in every cycle.
In addition, the hospital / clinic hygiene regulations must be observed.
Cleaning / disinfection
Cleaning and disinfection must be carried out immediately after use.
A mechanised process (disinfector) should be used for cleaning / disinfection. The efficiency of the process
used must be recognised and validated in principle (e.g. listed under disinfectants and disinfection proce-
dures tested and recognised by Robert-Koch-Institute / DGHM).
When using other procedures (e.g. a manual procedure), proof and process efficiency in principle must be
provided within the scope of validation.
Proof in principle of the suitability of the handles for efficient cleaning / disinfection was provided using a
cyclic cleaning system (Netsch-Bellmed T-600-IUDT/AN, programme 2 for small parts; code B).
It is not allowed to use agents / disinfectants, which contain the following substances, as these may cause
changes in the material:
- High-concentration organic and inorganic acids
- Chlorinated hydrocarbons
- 2-ethoxyethanol
* When occupying the disinfection zone (washing zone 2), the re-rinse and draining times will depend on
the respective objects being washed therein!
Sterilisation
Only previously cleaned and disinfected handles may be sterilised.
The handles are placed in a suitable sterilisation pack (one-way sterilisation pack, e.g. foil / paper sterilisa-
tion bags, single or double pack) in accordance with DIN EN 868 / ISO 11607 for steam sterilisation and
then sterilised.
Use only the sterilisation procedure listed below for sterilisation. Other sterilisation procedures (e.g. ethyl-
ene oxide, formaldehyde and low-temperature plasma sterilisation) are not permissible.
Proof in principle of the handles’ suitability for effective sterilisation was provided using a fractional vacuum
process (Euroselectomat 666 by MMM Münchner Medizin Mechanik GmbH, sterilising temperature 134°C,
holding time 7 min.)
Inspection / durability
The handles should be inspected for damage and changed before re-use, if required.
The handles may be cleaned / disinfected, sterilised and re-used for a maximum of 1000 times. If the han-
dles are re-used more than 1000 times, then this will be the responsibility of the hospital / clinic.
15
Alc. ≤ 20 %
antistatic, non-fluffy cloth.
6. Maintenance
The lamp has been designed and built so that regular maintenance intervals are not necessary.
In order to keep the system easy running throughout its life span we recommend that the hinges be
greased once a year with an acid-free grease.
The lamp body may only be dismantled from the spring arm in reverse order to its assembly after the as-
sembly locking device has been inserted and tightened since the arm is under spring tension.
Attention: Screw the transport safeguard into place in the spring arm before removing the lights.
♦ Height adjustment
Remark:
The halogen bulbs have a service life of ap-
prox. 1000 hours without any deterioration in
their luminosity.
X ATTENTION!
S The lamps may not be used without this filter.
14
S S
X
15
7. Data
7.1 Technical data
7.2 Wiring
1
2 N
3 L
P
Switch Toroid
transformer
Halogen bulb
0V 21V 23V
white red brown
secondary
primary
0V 120V 230V
black grey orange
Operation
Min. Max.
Temperature +10°C +40°C
Relative atmospheric humidity 30% 75%
Air pressure 700 hPa 1060 hPa
Transport / Storage
Min. Max.
Temperature -10°C +50°C
Relative atmospheric humidity 20% 90%
Air pressure 700 hPa 1060 hPa
8. Characteristics
Protective conductor
“
ON/OFF” switch
8.3 CE-mark
The products Mach 130 FP comply to the standards 93/42/EEC for medical products of
the European Community’s Council.
9. Disposal
The lamp does not contain any danger goods.
The components of the lamp should be properly disposed at the end of its shelf-life.
Make sure, that the materials are carefully separated.
31 10
11
48 17,18
13 3
4
47 30
12
8 1x 65
(spare part)
48
1
39
7
58
6
44
50
5
19
45
16
2
15
52,53 15 14
26,65
64 4
68
32,33,34
67
66
30 1x 65 38
1x 12
(spare part)