MDCG guidance
MDCG 2019-2: 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
MDCG guidance · Unique Device Identifier (UDI) · February 2019
Key facts
| Reference | MDCG 2019-2 |
|---|---|
| Title | 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 |
| Topic | Unique Device Identifier (UDI) |
| Published | February 2019 |
| Document | health.ec.europa.eu |
At a glance
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- MDCG 2019-2 (February 2019) Revisions on file
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About MDCG guidance documents
The Medical Device Coordination Group (MDCG), made up of EU member-state experts, endorses guidance on applying the Medical Devices Regulation (EU) 2017/745 and the In Vitro Diagnostic Regulation (EU) 2017/746. Each page here covers one document and all of its revisions.