Conmed 8730
Ref 8730
Conmed 8730 is a Class I device made by Conmed Corporation, registered in EUDAMED on 25 May 2026 (Basic UDI-DI B-10845854025505) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854025505), 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-10845854025505 10845854025505 | Date25 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10845854025505 | Date24 Sep 2020 | StatusListed |
Official records
- EUDAMED public site B-10845854025505
- AccessGUDID record 10845854025505
Across registries
- EUDAMED Basic UDI-DI B-10845854025505 registered 25 May 2026 Active
- FDA GUDID UDI-DI 10845854025505 listed 24 Sep 2020 Listed
Timeline
- Listed FDA GUDID 10845854025505
- Registered EUDAMED B-10845854025505
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conmed
- Generic name
- Fluted surgical drill bit, reusable
- Device name
- Reusable Manual Surgical Instruments
- Model / Ref / Catalog
- 8730
- Primary DI / UDI-DI
- 10845854025505
- Basic UDI-DI
- B-10845854025505
- FDA product code
- LXH
- EMDN code
- L091106 Instruments for the preparation of tissue implants in orthopaedic and traumatological surgery, reusable
- GMDN term
- Fluted surgical drill bit, 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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