Aesculap BH205R
Ref BH205R
Aesculap BH205R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI 40392390000030672L) and listed in FDA GUDID since 7 Jul 2020 (UDI-DI 04038653411542), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number40392390000030672L 04038653411542 | Date22 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04038653411542 | Date7 Jul 2020 | StatusListed |
Official records
- EUDAMED public site 40392390000030672L
- AccessGUDID record 04038653411542
Across registries
- EUDAMED Basic UDI-DI 40392390000030672L registered 22 Sep 2026 Active
- FDA GUDID UDI-DI 04038653411542 listed 7 Jul 2020 Listed
Timeline
- Listed FDA GUDID 04038653411542
- Registered EUDAMED 40392390000030672L
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Aesculap
- Generic name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable
- Device name
- Haemostatic clamp
- Model / Ref / Catalog
- BH205R
- Primary DI / UDI-DI
- 04038653411542
- Basic UDI-DI
- 40392390000030672L
- Direct marketing DI
- 04038653411542
- FDA product code
- HRQ
- EMDN code
- L031310 Dissection forceps, reusable
- GMDN term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization