Conmed 4.1003
Ref 4.1003
Conmed 4.1003 is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-10845854038185) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854038185), 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-10845854038185 10845854038185 | Date29 Apr 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10845854038185 | Date24 Sep 2020 | StatusListed |
Official records
- EUDAMED public site B-10845854038185
- AccessGUDID record 10845854038185
Across registries
- EUDAMED Basic UDI-DI B-10845854038185 registered 29 Apr 2026 Active
- FDA GUDID UDI-DI 10845854038185 listed 24 Sep 2020 Listed
Timeline
- Listed FDA GUDID 10845854038185
- Registered EUDAMED B-10845854038185
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conmed
- Generic name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable
- Device name
- Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
- Model / Ref / Catalog
- 4.1003
- Primary DI / UDI-DI
- 10845854038185
- Basic UDI-DI
- B-10845854038185
- FDA product code
- GEN
- EMDN code
- L090999 Orthopaedic surgery cutting instruments, reusable - other
- GMDN term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- 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
- Size
- Length — 130 MillimeterWidth — 3.4 Millimeter
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