Olympus CelonLab ENT Instructie

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Olympus CelonLab ENT Instructie
Product name:
Hardware version:
The unit must undergo a safety check at annual intervals in accordance with the national statutory regulations. Please follow these test
instructions. All tests must be done with fully functional and calibrated test equipment and by technicians trained in the service / maintenance
of electrical medical devices. Record the test results in the "safety check report" for reference in future tests and provide the user of the unit
with a signed report. If the unit fails to meet any of the checks, contact the manufacturer.
During service / maintenance take care of the different hardware versions which may be applicable (see below).
The hardware version of the unit can be identified by the serial number which can be found on the type plate at the back side of the unit. The
table below shows the serial number range to identify the hardware version.
Hardware version
Serial number (SN)
30 ... 31
A22701LE01.0001 ... A58702LE01.9999
32 ... ≥ 35
1000-1001 ... 6172-9999
From hardware version 35 the serial number itself includes already the hardware version. This code was introduced for units manufactured
since February 2005.
Example:
1234 W35 -567
Hardware version

Recommended test equipment and accessories

 Electrical safety tester (Example: Unimet 1000 ST, Bender)
 Electrosurgical analyzer (Example: QA-ES, Metron)
Load resistor 100 Ω, 25 W (or more), 5 % tolerance, low inductive part, short time load
 Connection cables, HF-output (banana) to electrosurgical analyzer or load resistor
 Power cord
 Footswitch
© Celon AG
,
Issue date: 01.09.2008
SCI.991007-1.4
Safety Check
Instruction.doc

Safety Check Instruction

CelonLab ENT (100...120 V~)
 30
REF no.: WB991007
LAB991.025.007
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