EUDAMED last updated this device on Jul 9, 2026
Henry Schein
B-H65810009951On the marketClass I
- Applicable legislation
- —
- Organization name
- Henry Schein 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 →- H65810009951
- Reference / catalog number
- 1000995
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.
Henry Schein is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Henry Schein Inc.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.