EU MDCG 2019-2:2019
Current
The latest, up-to-date edition.
Guidance on application of UDI rules to device-part of products referred to in Article 1(8), 1(9) and 1(10) of Regulation 745/2017
Hardcopy
English
01-02-2019
Article 1(8),1(9), 1(10) of the Medical Device Regulation (EU) 2017/745 (MDR) set the basic criteria to determine whether and to what extent the relevant legislation on medical devices, medicinal products, human tissue and cells apply to certain products containing a medical device part. In particular, “8.
| DocumentType |
Standard
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| Pages |
3
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| PublisherName |
European Union
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| Status |
Current
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