Product Manual

OPERATIONAL INFORMATION
The operational information contained in this section is intended for the customer review of regulatory issues. The
information pertains to the use of the products both domestically and internationally:
1. The smoke evacuator system complies with IEC601.1 electrical specifications in the following systems:
120V/60Hz, l00V/50Hz, 220V/50Hz, 240V/50Hz.
2. The smoke evacuator system has a classification under the UL2601-1, Clause 5.1 of: CLASS 1 Equipment.
3. The smoke evacuator system has an identification under the UL2601-1, Clause 5.2 according to the degree of
protection against electric shock: Type CF Equipment.
4. The smoke evacuator system has an identification under the UL2601-1, Clause 5.3 according to the degree of
protection against harmful ingress of water: Ordinary Equipment (enclosed equipment without protection against
ingress of water).
5. The smoke evacuator system has a classification under the UL2601-1, Clause 5.4 according to the method
of sterilization or disinfection recommended by Bovie Medical Corporation: Unplug the unit. Wipe the unit with
a damp cloth containing a mild disinfectant solution, or soapy water. Wipe the unit dry with a clean cloth. Do not
steam sterilize.
6. The smoke evacuator system has a classification under the UL2601-1, Clause 5.5 according to the degree of
safety of application in the presence of flammable anesthetic mixture with air or with oxygen or nitrous oxide:
Equipment not suitable for use in the presence of flammable anesthetic mixture with air or with oxygen or
nitrous oxide.
7. The smoke evacuator system has a classification under the UL2601-1, Clause 5.6 according to the mode of oper-
ation: Continuous Operation.
8. The fuses on the circuit board are to be serviced by an authorized Bovie Medical Corporation technician.
The smoke evacuator system and all filters and accessories are not intended for contact with patients.
4 Bovie Medical Corporation