EUDAMED last updated this device on Sep 1, 2026
BIOSILK
B-05944756512774On the marketClass IIb
- Applicable legislation
- —
- Organization name
- BIOSINTEX SRL
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 →- 05944756512774
- Reference / catalog number
- BX5034
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.
BIOSILK is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by BIOSINTEX SRL. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.