Landanger B123002
by Landanger
Ref B123002Model SCALPEL HANDLES, REUSABLE
Landanger B123002 is a scalpel handle (EU MDD Class I; FDA Class I; FDA product code DWS, Instruments, Surgical, Cardiovascular) made by Landanger, registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI B-03661219331698) and listed in FDA GUDID since 23 Sep 2022 (UDI-DI 03661219331698), active as of 23 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-03661219331698 03661219331698 | Date15 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03661219331698 | Date23 Sep 2022 | StatusListed |
Official records
- EUDAMED public site B-03661219331698
- AccessGUDID record 03661219331698
Across registries
- EUDAMED Basic UDI-DI B-03661219331698 registered 15 Oct 2026 Active
- FDA GUDID UDI-DI 03661219331698 listed 23 Sep 2022 Listed
Timeline
- Listed FDA GUDID 03661219331698
- Registered EUDAMED B-03661219331698
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Landanger
- Generic name
- Scalpel handle, reusable
- Model / reference
- B123002, SCALPEL HANDLES, REUSABLE
- Primary DI / UDI-DI
- 03661219331698
- Basic UDI-DI
- B-03661219331698
- Direct marketing DI
- 03661219331698
- FDA product code
- DWS
- EMDN code
- L010103 Handles for scalpels, reusable
- GMDN term
- Scalpel handle, reusable
- Device class
- Class I
- Regulation number
- 870.4500
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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