标准号: |
IEC 61010-2-101-2015 |
英文名称: |
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment |
中标分类: |
仪器仪表>>电工仪器、仪表综合 |
发布日期: |
2015-01 |
发布单位: |
IX-IEC |
标准状态: |
请与本站工作人员进行确认 |
ICS分类: |
0>>0 |
正文语言: |
双语(英,法) |
原文名称: |
Règles de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire - Partie 2-101: Exigences particulières pour les appareils médicaux de diagnostic in vitro (DIV) |
页数: |
37P.;A4 |
附注: |
History:IEC 61010-2-101 (2015-01);IEC 66/545/FDIS (2014-10);IEC 66/487/CDV (2012-08);IEC 61010-2-101 (2002-01);IEC 66/261/FDIS (2001-09);IEC 66/221/CDV (1999-04) |
被代替标准: |
IEC 66/545/FDIS-2014;IEC 61010-2-101-2002 |
引用标准: |
ISO 13857-2008;ISO 14971-2007;ISO 18113-5-2009 |
采用关系: |
ANSI/UL 61010-2-101-2015,IDT;CAN/CSA-C22.2 No. 61010-2-101-2015,MOD;UL 61010-2-101-2015,IDT |
内容提要(EN): |
Biological hazards;Control devices;Control equipment;Definitions;Diagnosis;Diagnostic equipment;Electric appliances;Electrical engineering;Hazards;In vitro;In-vitro diagnostic;Laboratory apparatus;Laboratory medicine;Laboratory ware;Measuring instruments;Medical equipment;Protective measures;Risk analysis;Safety;Safety requirements;Specification (approval);Testing |
内容提要(QT): |
Anforderung;Begriffe;Biogefahrdung;Definition;Diagnostik;Diagnostikgerat;Elektrogerat;Elektrotechnik;Gefahrdung;in vitro;In-vitro-Diagnostik;Laboratoriumsgerat;Laborgerat;Labormedizin;medizinische Ausstattung;medizinisches Gerat;Messgerat;Prufung;Prufverfahren;Regelgerat;Risikoanalyse;Schutzmasnahme;Sicherheit;Sicherheitsanforderung;Steuergerat |
归属: |
国际 |