Breaking News

Main Menu

Ansi Aami He75 2009 Edition Nfpa

понедельник 28 января admin 18
Ansi Aami He75 2009 Edition Nfpa Rating: 5,8/10 9960 votes

American national standard ansi/aami he75:2009/(r)2013 (revision of ansi/aami he48:1993) human factors engineering - design of medical devices developed by association for the advancement of medical instrumentation. NFPA (Fire) 54 / ANSI Z223.1,National Fuel Gas Code. 2009 Edition, Includes Amendment A. AAMI Standard: AASHTO Standard. The American National Standards Institute (ANSI, /. 2009 ANSI announced a product and services agreement with Citation Technologies to.

Scope: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1. NOTE 1 See also 4.2. Nfs most wanted all 100 unlock all city savegames fils pc.

The IEC 60601 series does not apply to: - in vitro diagnostic equipment that does not fall within the definition of ME EQUIPMENT is covered by the IEC 61010 series [61]; - implantable parts of active implantable medical devices covered by the ISO 14708 series [69]; or - medical gas pipeline systems covered by ISO 7396-1 [68]. NOTE 2 ISO 7396-1 applies the requirement of IEC 60601-1-8 to certain monitoring and ALARM SIGNALS.

Catalog:Glossary of equivalent standards lowing annexes (J and K) after Annex I. Committee representation Acknowledgments Foreword 1 Scope 2 Applicability and use 3 Normative references 4 Definitions 5 General requirements 5.1 Quality systems 5.2 Test methods 5.3 Sampling 6 Design inputs 7 Selection and evaluation of materials 7.1 Sterilization requirements (ANSI/AAMI/ISO11607-1: 2006, 5.1.6(e) and 5.3)) 7.2 Safety requirements (ANSI/AAMI/ISO 11607-1:2006, 5.1.5 and 5.1.6) 7.3 Barrier requirements.