Notices - Vyaire SprintPack Manual Del Usuario

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
Vyaire Medical's European Representative for vigilance reporting within the
European Community is:
Authorized Representative in the
European Community
Emergo Europe
Prinsessegracht 20
2514 AP The Hague
The Netherlands
Any product malfunctioning issues that fall under Medical Device Directives
Essential Requirements should be directed to Emergo Europe.
32328-001 Version A
Operator's Manual – SprintPack
™
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