Guide Wire Dispenser 2231-1000
Guide Wire Dispenser 2231-1000 is a Class I device made by Captiva Spine, listed in FDA GUDID since 23 Jul 2022 (UDI-DI M73922311000), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM73922311000 | Date23 Jul 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Guide Wire Dispenser
- Generic name
- Guidewire holder
- Model / reference
- 2231-1000
- Primary DI / UDI-DI
- M73922311000
- FDA product code
- LXH
- GMDN term
- Guidewire holder
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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