Q&A on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746

European Union · Last verified: 2026-09-08

Number
MDCG 2021-26
Type
Guidance
Issuer
Medical Device Coordination Group (MDCG)
Status
in_force
Authority
欧盟委员会 / MDCG

What this covers

MDCG 指南文件,属「Authorised Representatives, Importers, Distributors」专题,委员会指南清单页标注的发布时间为 October 2021;内容为「Q&A on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746」。此类文件无强制法律效力,但代表成员国主管当局与公告机构对 MDR/IVDR 的共同解释口径。注意 effective 填的是发布月份(日补 01),不是法律生效日。

Official text: https://health.ec.europa.eu/document/download/4c7bd740-d7c3-4f7b-9a4d-249121a6

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Facts only; not legal advice. The official current text prevails.