Dinamap Pro 100V2 Spécifications télécharger pdf (Page 10)

Product Compliance

The DINAMAP

PRO Monitor is classified in the following

categories for compliance with IEC 601-1:

• Class l, internally powered

•Transportable

• For continuous operation

• Not suitable for use in the presence of flammable

anesthetics

• Not for use in the presence of an oxygen-enriched

atmosphere (oxygen tent)

• Type BF applied parts

• IPX1, degree of protection against ingress of water

• Sterilization/Disinfection, see Appendix F

DINAMAP

PRO MONITOR

CLASSIFIED WITH RESPECT TO ELECTRIC SHOCK, FIRE

AND MECHANICAL AND OTHER SPECIFIED HAZARDS

ONLY IN ACCORDANCE WITH CAN/CSA C22.2 NO.

601.1. ALSO EVALUATED TO IEC-601-2-30.

0086

This product conforms with the essential requirements

of the Medical Device Directive. Accessories without

the CE mark are not guaranteed to meet the Essential

Requirements of the Medical Device Directive.

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Dinamap Pro 100V2 Spécifications Page 10