Canon CX-1 - Manual (Page 3)

-3-
Safety Information
Regulations
This instrument conforms to IEC 60601-1-2:2001/A1:2004 and IEC 60601-1-2:2007.
For USA and Canada
• When the CX-1 is going to be operated at a voltage of 240V in USA or Canada, be sure to con-
nect the instrument to a center tapped voltage source.
• This instrument is CLASS I EQUIPMENT according to UL 60601-1 and CAN/CSA C22.2
No. 601.1.
• Grounding reliability can only be achieved when the equipment is connected to an equivalent
receptacle marked “Hospital Only” or “Hospital Grade”.
• The following mark indicates that the instrument is Type B Applied Parts (forehead rest and chin
rest).
• The degree of protection against ingress of water is IPX0.
• This equipment is not suitable for use in the presence of a flammable anaesthetic mixture with
air, oxygen or nitrous oxide.
• The mode of operation is Continuous Operation.
For EU Countries
• The following mark shows compliance of the instrument with Directive 93/42/EEC.
• This instrument is CLASS I EQUIPMENT according to EN 60601-1:2006 and IEC 60601-1:2005.
• The following mark indicates that the instrument is Type B Applied Parts (forehead rest and chin
rest) according to EN 60601-1.
• The degree of protection against ingress of water is IPX0.
• This equipment is not suitable for use in the presence of a flammable anaesthetic mixture with
air, oxygen or nitrous oxide.
• The mode of operation is Continuous Operation.
Für Deutschland
• Während des Betriebs liegt der Schalldruckpegel dieses Instruments bei 70 dB(A) oder weniger
gemäß ISO 7779.
MEDICAL EQUIPMENT WITH RESPECT TO ELECTRICAL SHOCK,
FIRE AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH UL 60601-1 and CAN / CSA C22.2 No. 601.1
41C4
000_L-IE-5169D_CX-1.book Page 3 Monday, July 29, 2013 10:42 AM