Landanger J758200
by Landanger
Ref J758200Model BONE CUTTERS, REUSABLE
Landanger J758200 is a Class I device made by Landanger, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-03661219082811) and listed in FDA GUDID since 1 Aug 2023 (UDI-DI 03661219082811), active as of 24 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-03661219082811 03661219082811 | Date16 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03661219082811 | Date1 Aug 2023 | StatusListed |
Official records
- EUDAMED public site B-03661219082811
- AccessGUDID record 03661219082811
Across registries
- EUDAMED Basic UDI-DI B-03661219082811 registered 16 Oct 2026 Active
- FDA GUDID UDI-DI 03661219082811 listed 1 Aug 2023 Listed
Timeline
- Listed FDA GUDID 03661219082811
- Registered EUDAMED B-03661219082811
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Landanger
- Generic name
- Wire cutter
- Model / reference
- J758200, BONE CUTTERS, REUSABLE
- Primary DI / UDI-DI
- 03661219082811
- Basic UDI-DI
- B-03661219082811
- FDA product code
- DWS
- EMDN code
- L090901 Bone cutters, reusable
- GMDN term
- Wire cutter
- 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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