EUDAMED last updated this device on Aug 17, 2026
Flexicare
B-05023323028969- Applicable legislation
- —
- Organization name
- Flexicare Medical Limited
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 05023323028969
- Reference / catalog number
- 3109753
Flexicare is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Flexicare Medical Limited. Placed on the EU market in Northern Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.