Conmed C9863
Ref C9863
Conmed C9863 is a foot-switch (EU MDR Class I; FDA Class I; FDA product code HWE, Instrument, Surgical, Orthopedic, Ac-Powered Motor and Accessory/Attachment) made by Conmed Corporation, registered in EUDAMED on 28 Oct 2025 (Basic UDI-DI 084585464940F3) and listed in FDA GUDID since 28 Apr 2020 (UDI-DI 10845854034552), active as of 23 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number084585464940F3 10845854034552 | Date28 Oct 2025 | StatusActive |
| United States | GUDID listing GUDID | Number10845854034552 | Date28 Apr 2020 | StatusListed |
Official records
- EUDAMED public site 084585464940F3
- AccessGUDID record 10845854034552
Across registries
- EUDAMED Basic UDI-DI 084585464940F3 registered 28 Oct 2025 Active
- FDA GUDID UDI-DI 10845854034552 listed 28 Apr 2020 Listed
Timeline
- Listed FDA GUDID 10845854034552
- Registered EUDAMED 084585464940F3
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conmed
- Generic name
- Foot-switch, electrical
- Device name
- Orthopedic, Non-active, Accessory, Footswitch, Electric
- Model / Ref / Catalog
- C9863
- Primary DI / UDI-DI
- 10845854034552
- Basic UDI-DI
- 084585464940F3
- Direct marketing DI
- 20845854034559
- FDA product code
- HWE
- EMDN code
- Z129099 Various instruments for functional exploration and therapeutic interventions - other
- GMDN term
- Foot-switch, electrical
- Device class
- Class I
- Regulation number
- 878.4820
- EU registration type
- Standard device
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
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