87
GB
1505093, Edition 2012-05, Version 5
8 Dismantling / Mounting in Case of Service
Figure 12: Version with 7/9-pole plug cou-
pling
Only for version with 7/9-pole plug coupling
(See "Figure 12")
Connecting the plugs
1. Connect the 6-pole plug 4.
2. Screw 3 plug adapters 5 into each other in accordance with the colour code.
3. Gently push the 6-pole plug 4 and the 3 plug adapters 5 into the spring arm 4.
Mounting the end device
4. Grease the pivot groove and the pivot 3 using a suitable friction bearing grease
(e.g. Microgleit GP 360).
5. Position the pivot 3, keeping it straightly aligned, and establish the assembly con-
nection 3 by gently pushing towards the spring arm 4.
Completing the installation
(See "Figure 12")
End device crashing
When using an incorrect securing segment 5 the end device (e.g. OR
lamp) can crash and the spring arm 4 can suddenly jump upwards:
• Only use a genuine securing segment 5.
1. Insert the genuine securing segment 5, unscrew the sleeve securing screw M3 x
8mm 2 and push the sleeve 1 downwards.
End device crashing
The sleeve 1 secures the securing segment 5 and thus ensures that the
end device in the spring arm 4 is securely in place:
• Check that the sleeve 1 covers the securing segment 3.
• Secure the sleeve 1 using the sleeve securing screw M3 x 8mm 2.
2. Tighten the sleeve securing screw M3 x 8mm 2 again.
3. Check that the end device (e.g. OR lamp) is securely in place.
Extending the vertical lift
4. If required, extend the vertical lift of the spring arm 4 as described in
“Chapter
9.4.1” on page 100
.
Adjustments
5. Adjust the brake force and spring tension as described in
“Chapter 9” on page 95
.
Function test
6. Connect the system to the mains.
7. Perform a function test.
ACROBAT 2000 appliances are only intended for the connection of luminaires for medical
diagnosis, surgical luminaires and flat screens bearing the CE mark and with a maximum
payload of 21 kg.
For technical assistance for creating a medical-electrical (ME) system refer to
DIN EN 60601-1, Part 16.
The manufacturer / marketer of the ME system must provide a declaration in accordance
with Article 12 of 93/42/EEC (Medical Device Directive, MDD).
1WARNING
1WARNING
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