EUDAMED last updated this device on Sep 11, 2026
Arthrex®
0888867HedLesScrw000000AUOn the marketClass IIb
- Applicable legislation
- —
- Organization name
- Arthrex Inc.
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 →- 00888867125902
- Reference / catalog number
- AR-8643-24
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
Arthrex® is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Arthrex Inc.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.