SprintPack Operator's Manual - AARC.org

NoticesThe SprintPack Li-Ion Power System may emit and receive electromagneticinterference. Avoidance of this exposure is recommended wheneverpossible.European Regulatory Requirements per 93/42/EEC MedicalDevice DirectivesPulmonetic Systems’ European Representative for vigilance reporting withinthe European Community is:MediMark® Europe Sarl.11, rue Emile Zola. BP 2332F-38033 Grenoble Cedex 2. FranceTel: +33 (0)4 76 86 43 22Fax: +33 (0)4 76 17 19 82E-mail: info@medimark-europe.comAny product malfunctioning issues that fall under Medical Device DirectivesEssential Requirements should be directed to MediMark.18415-001, Rev. B Operator’s Manual - SprintPack 1-5