PHILIPS MEDICAL SYSTEMS
C-2
Meets the requirements of the applicable European
Directives, including RoHS Directive 2011/65/EU, The
Restriction of the Use of Certain Hazardous Sub-
stances in Electrical and Electronic Equipment.
Meets the requirements of the European Medical
Device Directive 93/42/EEC. The four numerical digits
indicate the identification number of the Notified Body
involved in assessing the product’s conformity with the
directive.
Device manufacturer.
Indicates the AHA/ERC/ILCOR resuscitation Guide-
lines version for which the device is optimized
(expressed as a year).
Certified by the Canadian Standards Association.
Reference order number.
Authorized EU representative.
Expiration date.
Lithium manganese dioxide battery.
One battery in package.
Do not crush the battery.
Do not expose the battery to high heat or open flames.
Do not incinerate the battery.
Do not mutilate the battery or open the battery case.
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