Conmed 8750
Ref 8750
Conmed 8750 is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-10845854025659) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854025659), 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-10845854025659 10845854025659 | Date29 Apr 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10845854025659 | Date24 Sep 2020 | StatusListed |
Official records
- EUDAMED public site B-10845854025659
- AccessGUDID record 10845854025659
Across registries
- EUDAMED Basic UDI-DI B-10845854025659 registered 29 Apr 2026 Active
- FDA GUDID UDI-DI 10845854025659 listed 24 Sep 2020 Listed
Timeline
- Listed FDA GUDID 10845854025659
- Registered EUDAMED B-10845854025659
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conmed
- Generic name
- Soft-tissue surgical hook, reusable
- Device name
- Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
- Model / Ref / Catalog
- 8750
- Primary DI / UDI-DI
- 10845854025659
- Basic UDI-DI
- B-10845854025659
- FDA product code
- LXH
- EMDN code
- L03130401 Tissue and organ grasping forceps, reusable
- GMDN term
- Soft-tissue surgical hook, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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