EUDAMED last updated this device on Jul 8, 2026
Tycheseal™
B-06957485010021On the marketClass III
- Applicable legislation
- —
- Organization name
- Beijing Percutek Therapeutics 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 →- 06957485010021
- Reference / catalog number
- PABF2212110
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.
Tycheseal™ is an EU-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by Beijing Percutek Therapeutics Inc.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.