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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- 발행일 : 2018-10-05
- 발행기관 : IEC
상세정보
| 분야 | TC 66 : Safety of measuring, control and laboratory equipment |
|---|---|
| 적용범위 | 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: - adaptation of changes introduced by Amendment 1 of IEC 61010-1; - added tolerance for stability of AC voltage test equipment to Clause 6. This Part 2-101 is intended to be used in conjunction with IEC 61010-1. It was established on the basis of the third edition (2010) and its Amendment 1 (2016). |
| 국제분류(ICS)코드 |
19.080 : 전기 및 전자 시험 및 측정기구
11.040.55 : 진단장비 |
| 페이지수 | 34 |
| 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
- ISO 14971:2019 - Medical devices — Application of risk management to medical devices
- IEC 62366-1:2015 - Medical devices - Part 1: Application of usability engineering to medical devices
- IEC 61010-2-081:2019 - Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-081: Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes
- KS P IEC 62304 - 의료기기 소프트웨어 — 소프트웨어 수명주기 프로세스
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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