Notices - CareFusion SprintPack Bedienungsanleitung

Notices

The SprintPack Li-Ion Power System may emit and receive electromagnetic
interference. Avoidance of this exposure is recommended whenever
possible.
European Regulatory Requirements per 93/42/EEC Medical
Device Directives
CareFusion's European Representative for vigilance reporting within the
European Community is:
CareFusion Respiratory Systems GMBH
Leibnizstrasse 7
97204 Hoechberg, Germany
Tel: 49.931.4972.0
Fax: 49.931.4972.423
Email: support.vent.eu@carefusion.com
Any product malfunctioning issues that fall under Medical Device Directives
Essential Requirements should be directed to CareFusion Respiratory
Systems GMBH.
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18415-001, Rev. E Operator's Manual - SprintPack™