EUDAMED last updated this device on Jul 1, 2026
BIOTEQ
B-04712954421331On the marketClass IIa
- Applicable legislation
- —
- Organization name
- Bioteque Corporation
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 →- 04712954421331
- Reference / catalog number
- BT-PD1-1235-W
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.
BIOTEQ is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Bioteque Corporation. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.