MDCG guidance

MDCG 2019-1: MDCG guiding principles for issuing entities rules on basic UDI-DI

MDCG guidance · Unique Device Identifier (UDI) · January 2019

Key facts

Reference MDCG 2019-1
Title MDCG guiding principles for issuing entities rules on basic UDI-DI
Topic Unique Device Identifier (UDI)
Published January 2019
Document health.ec.europa.eu

At a glance

  • Yes Full text searchable in Orca1
  • MDCG 2019-1 (January 2019) Revisions on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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.

Source: European Commission, Medical Device Coordination Group (MDCG) endorsed documents and other guidance. © European Union, reused under Commission Decision 2011/833/EU

Browse all MDCG guidance documents