5805-0-225
5805-0-225 is a Class I device made by Stryker Corp., listed in FDA GUDID since 7 Apr 2020 (UDI-DI 04546540007797), 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 | Number04546540007797 | Date7 Apr 2020 | StatusListed |
Official records
- AccessGUDID record 04546540007797
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Fluted surgical drill bit, single-use
- Model / Ref / Catalog
- 5805-0-225
- Primary DI / UDI-DI
- 04546540007797
- FDA product code
- LXH
- GMDN term
- Fluted surgical drill bit, single-use
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 180.0 Millimeter
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