Instrument 6210-3-400
Ref 6210-3-400Model 08858251004909TX
Instrument 6210-3-400 is a device classified as Class IIa in the EU and Class I in the US made by Howmedica Osteonics Corp., registered in EUDAMED on 13 Oct 2026 (Basic UDI-DI 08858251004909TX) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613327144123), 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 | Number08858251004909TX 07613327144123 | Date13 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327144123 | Date24 Sep 2016 | StatusListed |
Official records
- EUDAMED public site 08858251004909TX
- AccessGUDID record 07613327144123
Across registries
- EUDAMED Basic UDI-DI 08858251004909TX registered 13 Oct 2026 Active
- FDA GUDID UDI-DI 07613327144123 listed 24 Sep 2016 Listed
Timeline
- Listed FDA GUDID 07613327144123
- Registered EUDAMED 08858251004909TX
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Gray EUDAMEDInstrument GUDID
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device name
- TF-030 - Class IIa - Hook - Gamma
- Model / Ref / Catalog
- 6210-3-400, 08858251004909TX
- Primary DI / UDI-DI
- 07613327144123
- Basic UDI-DI
- 08858251004909TX
- FDA product code
- LXH
- EMDN code
- P091399 Orthopaedic implant instruments, single-use - other
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 10.0 MillimeterLength — 250.0 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
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