Canon CF-1 - Manual (Page 3)

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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 CF-1 is going to be operated at a voltage of 240V in USA or Canada, be sure to
connect the instrument to a center tapped voltage source.
• This instrument is CLASS I EQUIPMENT according to UL60601-1.
• Grounding reliability can only be achieved when the equipment is connected to an equiva-
lent 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.
WITH RESPECT TO ELETRIC SHOCK, FIRE MECHANICAL
AND OTHER SPECIFIED HAZARDS ONLY IN
ACCORDANCE WITH CAN/CSA C22.2 NO. 601.1,
MEDICAL EQUIPMENT CERTIFIED FOR CANADA
MEDICAL EQUIPMENT WITH RESPECT
TO ELETRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL60601-1
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