KLS Martin group marLED E3 - Notices Concerning the Inspection Plan

Service Manual
Operating Lights marLED® E3, E9, E9i, E15, battery and
marLED® E3 on ceiling tube Ø 110 mm
136 Revision 2
13.3.2 Notices Concerning the Inspection Plan
The inspection plan is based on the standards:
• IEC 60601-2-41: “Particular Requirements for the Safety of Surgical Luminaires and Luminaires for
Diagnosis”.
• IEC 62353 “Medical electrical equipment – Recurrent test and test after repair of medical electrical
equipment”
• A separate Test Report form must be completed for each terminal device (light, surgiCam, TFT
suspension, etc.).
• This means that 4 forms must be filled out for an operating room using the following combination:
marLED® E9i, E15, surgiCam and TFT suspension:
– In the first form, underline marLED® E9i, four and ceiling.
– In the second form, underline marLED® E15, four and ceiling.
– In the third form, underline surgiCam, four and ceiling.
– In the fourth form, underline TFT, four and ceiling.
• Under Extras, enter any additional equipment or equipment deviating from the standard. Example:
surgiCam installed in light head.
• Be sure to specify the room or OR number and the serial number in each case.
• Under Customer and Company, enter the required details (incl. complete address) in capital letters. Do
not use a stamp!
• If the control activities are carried out by personnel of the Martin Service Center, 3 versions of the
inspection plan are to be created, where:
– The original always remains with the customer/operator of the devices.
– One copy is intended for the service personnel.
– One copy must be sent to the Gebrüder Martin.