Implantable Medical Devices Factsheet π
The #EC has released a factsheet for manufacturers of implantable medical devices and related to the application of Article 18 of Regulation (EU) 2017/745.
Key Points:
- Implantable devices will require an βImplant Cardβ IC, giving patients quick access to all relevant information for their device
- Information includes: Device Name, Type, UDI, Serial Number, Manufacturer Details, and patient details.
- The Factsheet outlines other requirements, including IC size, use of symbols, language, etc.
π https://ec.europa.eu/health/sites/default/files/md_topics-interest/docs/md_implany-cards_factsheet_en.pdf
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