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11
Introduction
•The mode of operation: Continuous Operation
The equipment is not suitable for use in the presence of a flammable anesthetic mixture with air
or with oxygen or nitrous oxide: Not AP or APG Category.
CE Doc
Declaration of conformity
This device complies with the requirements set out in the Council Directives on the
harmonization of the Laws of Member States concerning Medical Device Directive 93/42/EEC
as amended by 2007/47/EC with the compliance of conformity assessment Annex VII to be
self-declaration, the Restriction of The Use of Certain Hazardous Substances in Electrical And
Electronic Equipment Directive (2011/65/EU), Turkish EEE and ErP Directive, Commission
Regulation (EC) No 1275/2008 implementing Directive 2005/32/EC of the European Parliament
and of the Council with regard to ecodesign requirements for standby and off mode electric
power consumption of electrical and electronic household and office equipment, and the
Directive 2009/125/EC of the European parliament and of the council establishing a framework
for the setting of ecodesign requirements for energy-related products.