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Instructions for use
Fulfils the requirements of Directives 93/42/EEC and RoHS, REACH and
WEEE.
Medical Device
SGS listing marking according to US and Canadian standards (ANSI/AAMI
ES60601-1 and CAN/CSA C22.2 No. 60601- 1).
Date of manufacture (Standard ISO 7000).
Type B applied part (Standard IEC 60417).
Separate collection for electrical and electronic equipment according to
Directive 2012/19/EU (WEEE).
Consult electronic instructions for use (Standard ISO 7000-1641).
Refer to instruction manual/booklet (Standard ISO 7010).
Emergency stop (Standard IEC 60417)
Warning: Electricity (Standard ISO 7010).
To avoid risk of electric shock, this equipment must only be connected to a
supply mains with protective earth.
Electrostatic sensitive device (Standard IEC 60417)
Warning, hot surface (Standard ISO 7010).
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KaVo ProXam
3
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