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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 | 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 |
| 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
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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
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