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Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
| 분야 | |
|---|---|
| 적용범위 | IEC 61010-2-101:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition. IEC 61010-2-101:2018 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety publication, as specified in IEC Guide 104. This document has been prepared in close collaboration with Working Group CENELEC BTTF 88.1. This third edition cancels and replaces the second edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition: |
| 국제분류(ICS)코드 |
19.080 : 전기 및 전자 시험 및 측정기구
11.040.55 : 진단장비 |
| 페이지수 | 52 |
| Edition | 3.0 |
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | IEC 61010-2-101:2018 RLV | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment | 2018-10-05 | 표준 |
| 2 | IEC 61010-2-101:2018 | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment | 2018-10-05 | 표준 |
| 3 | IEC 61010-2-101:2015 | Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment | 2015-01-23 | 구판 |
| 4 | IEC 61010-2-101:2015 RLV | Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment | 2015-01-23 | 구판 |
| 5 | IEC 61010-2-101:2002 | Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment | 2002-01-09 | 구판 |
IEC 61010-2-031:1993 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-031: Particular requirements for hand-held probe assemblies for electrical measurement and test 상세보기
IEC 61010-2-041:1995 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-041: Particular requirements for autoclaves using steam for the treatment of medical materials, and for laboratory processes 상세보기
IEC 61010-2-043:1997 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-043: Particular requirements for dry heat sterilizers using either hot air or hot inert gas for the treatment of medical materials, and for laboratory processes 상세보기
IEC 61010-2-042:1997 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-042: Particular requirements for autoclaves and sterilizers using toxic gas for the treatment of medical materials, and for laboratory processes 상세보기
IEC TR 61010-3-010:1999 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 3-010: Conformity verification report for IEC 61010-2-010, Particular requirements for laboratory equipment for the heating of materials 상세보기
IEC 61010-1:2010+AMD1:2016 CSV - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements 상세보기
IEC 61326-2-6:2020 RLV - Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment 상세보기
IEC 62304:2006+AMD1:2015 CSV - Medical device software - Software life cycle processes 상세보기
IEC TR 62366-2:2016 - Medical devices - Part 2: Guidance on the application of usability engineering to medical devices 상세보기
BS EN ISO 14971:2019 - TC - Tracked Changes. Medical devices. Application of risk management to medical devices. 상세보기
IEC TS 63134:2020 - Active assisted living (AAL) use cases 상세보기
IEC 60034-5:2020 RLV - Rotating electrical machines - Part 5: Degrees of protection provided by the integral design of rotating electrical machines (IP code) - Classification 상세보기
KS B ISO TS 25740-1 - 에스컬레이터 및 무빙워크에 대한 안전요건 — 제1부: 세계공통 필수 안전요건(GESRs) 상세보기
KS B ISO TS 8100-21 - 승객 및 화물 운송용 엘리베이터 —제21부: 세계공통 필수안전요건(GESRs)을 충족하는 세계공통 안전 파라미터(GSPs) 상세보기
KS C IEC TS 62872 - 산업 시설과 스마트 그리드 사이의 산업 공정 측정, 제어 및 자동화 시스템 인터페이스 상세보기
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