Q&A on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746
- 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。
Facts only; not legal advice. The official current text prevails.