devemed 2811-00
by devemed GmbH
Ref 2811-00
devemed 2811-00 is a Class I device made by devemed GmbH, registered in EUDAMED on 9 Jul 2026 (Basic UDI-DI 4061644PG01040325) and listed in FDA GUDID since 15 Apr 2020 (UDI-DI 04061644020157), active as of 24 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 | Number4061644PG01040325 04061644020157 | Date9 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04061644020157 | Date15 Apr 2020 | StatusListed |
Official records
- EUDAMED public site 4061644PG01040325
- AccessGUDID record 04061644020157
Across registries
- EUDAMED Basic UDI-DI 4061644PG01040325 registered 9 Jul 2026 Active
- FDA GUDID UDI-DI 04061644020157 listed 15 Apr 2020 Listed
Timeline
- Listed FDA GUDID 04061644020157
- Registered EUDAMED 4061644PG01040325
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- devemed
- Generic name
- Chisel/osteotome blade handle
- Device name
- Handles for Chisel and Osteotome attachements
- Model / reference
- 2811-00
- Description
- Handle "Palti" for osteotom- & bone pusher attachment H-Type A
- Primary DI / UDI-DI
- 04061644020157
- Basic UDI-DI
- 4061644PG01040325
- Direct marketing DI
- 04061644020157
- FDA product code
- EMM
- EMDN code
- L150103 Dental osteotome blades, reusable
- GMDN term
- Chisel/osteotome blade handle
- Device class
- Class I
- Regulation number
- 872.4565
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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