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发表于 2022-7-28 08:47:43
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你确定原文说的是 “需要增加对MDR 第120条(3)以及第90/385/EEC号指令、第93/42/EEC号指令相应要求的理解且能执行落地的” 这个意思? 
我个人对下面的理解哈:MDR关于PMS的全部要求,对在210526前拿证且有效的MDD证书内产品均适用,如果想继续保持MDD证书有效的话,且MDD证书内的产品不发生significant change(这个的定义有指南的)。
3. By way of derogation from Article 5 of this Regulation, a device which is a class I device pursuant to Directive 93/42/EEC, for which the declaration of conformity was drawn up prior to 26 May 2021 and for which the conformity assessment procedure pursuant to this Regulation requires the involvement of a notified body, or which has a certificate that was issued in accordance with Directive 90/385/EEC or Directive 93/42/EEC and that is valid by virtue of paragraph 2 of this Article, may be placed on the market or put into service until 26 May 2024, provided that from 26 May 2021 it continues to comply with either of those Directives, and provided there are no significant changes in the design and intended purpose. However, the requirements of this Regulation relating to post-market surveillance, market surveillance, vigilance, registration of economic operators and of devices shall apply in place of the corresponding requirements in those Directives.
Without prejudice to Chapter IV and paragraph 1 of this Article, the notified body that issued the certificate referred to in the first subparagraph shall continue to be responsible for the appropriate surveillance in respect of all of the applicable requirements relating to the devices it has certified. |
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