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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- 발행일 : 2018-10-05
- 발행기관 : IEC
-
레드라인이란?
* RLV (Red-Line Version) : 구판과 최신판의 변경 사항을 빨간펜으로 표시해서 비교할 수 있게 만든 버전
* CMV (Commented version) : 표준의 개정 시 변경 부분(레드라인)에 대한 코멘트(메모)가 추가된 버전
* RLV 혹은 CMV를 구입하시면 최신판(Final version)은 별도로 구매하지 않아도 됩니다.
상세정보
| 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 |
이력정보
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | IEC 61010-2-101:2018 RLV상세보기 | 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 61010-2-101:2018상세보기 | 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 61010-2-101:2015상세보기 | 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 RLV상세보기 | 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 61010-2-101:2002상세보기 | 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 |
관련상품
- 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
- 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
- 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
- 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
- IEC TR 61010-3-061:1999 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 3-061: Conformity verification report for IEC 61010-2-061, Particular requirements for laboratory atomic spectrometers with thermal atomization and ionization
다른 사람이 함께 구입한 상품
- IEC 61010-1:2010+AMD1:2016 CSV - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
- 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
- BS EN 61010-2-010:2014 - Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for laboratory equipment for the heating of Materials.
- ISO 15223-1:2021 - Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements
- ISO 14971:2019 - Medical devices — Application of risk management to medical devices
추천 상품
- IEC TS 63134:2020 - Active assisted living (AAL) use cases
- 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
- KS B ISO TS 25740-1 - 에스컬레이터 및 무빙워크에 대한 안전요건 — 제1부: 세계공통 필수 안전요건(GESRs)
- KS B ISO TS 8100-21 - 승객 및 화물 운송용 엘리베이터 —제21부: 세계공통 필수안전요건(GESRs)을 충족하는 세계공통 안전 파라미터(GSPs)
- KS C IEC TS 62872 - 산업 시설과 스마트 그리드 사이의 산업 공정 측정, 제어 및 자동화 시스템 인터페이스
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