Two Striper PODIATRY BUR TAPER
Two Striper PODIATRY BUR TAPER (CFMDPDOC030) is a Class I device made by Abrasive Technology LLC, listed in FDA GUDID since 25 May 2021 (UDI-DI B868CFMDPDOC0300), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB868CFMDPDOC0300 | Date25 May 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Two Striper
- Generic name
- Podiatric bur, reusable
- Model / Ref / Catalog
- PODIATRY BUR TAPER, CFMDPDOC030
- Primary DI / UDI-DI
- B868CFMDPDOC0300
- FDA product code
- GFF
- GMDN term
- Podiatric bur, reusable
- Device class
- Class I
- Regulation number
- 878.4820
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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