Arthrex® AR-4206
Arthrex® AR-4206 is a Class I device made by Arthrex, Inc., listed in FDA GUDID since 3 Dec 2021 (UDI-DI 10888867033464), 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 | Number10888867033464 | Date3 Dec 2021 | StatusListed |
Official records
- AccessGUDID record 10888867033464
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Arthrex®
- Generic name
- Fluted surgical drill bit, single-use
- Model / Ref / Catalog
- AR-4206
- Primary DI / UDI-DI
- 10888867033464
- FDA product code
- MDM
- GMDN term
- Fluted surgical drill bit, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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