Arthrex® AR-9953DB-25S
Arthrex® AR-9953DB-25S is a Class I device made by Arthrex, Inc., listed in FDA GUDID since 17 Jun 2025 (UDI-DI 00888867504745), 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 | Number00888867504745 | Date17 Jun 2025 | StatusListed |
Official records
- AccessGUDID record 00888867504745
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- Withdrawn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-9953DB-25S
- Primary DI / UDI-DI
- 00888867504745
- FDA product code
- HTW
- GMDN term
- Fluted surgical drill bit, single-use
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
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