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Specifies the intended applications for ablation and coagulation of soft tissue in ENT surgery.
Details conditions where electrosurgical interventions are not recommended due to potential negative patient effects.
Outlines the unit's capabilities, including bipolar output and acoustic monitoring of coagulation status.
Explains the function of each control on the front and back panels of the power control unit.
Instructions for connecting the unit to the power supply system, ensuring cable quality and correct socket.
Details connecting the unit to the equipotential bonding system for increased electrical safety in the treatment room.
Information on the unit's drip-proof housing (IP 21) and the watertight footswitch (IP 68).
Step-by-step functional test procedure required before the unit is used for the first time.
Procedure for replacing external power fuses and caution regarding unauthorized internal fuse changes.
Guidance on reporting defects and ensuring repairs are performed by authorized technicians.
Requirement for yearly safety checks by authorized personnel according to national regulations.
Instructions for proper disposal of the unit and its components, following national and local guidelines.
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