Dentech 30060600
Dentech 30060600 is a Class I device made by Dentech Corporation, listed in FDA GUDID since 24 Sep 2020 (UDI-DI 04560218681997), registry data as of 12 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 | Number04560218681997 | Date24 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 04560218681997
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dentech
- Generic name
- Bone trephine, reusable
- Model / reference
- 30060600
- Primary DI / UDI-DI
- 04560218681997
- FDA product code
- EJL
- GMDN term
- Bone trephine, reusable
- Device class
- Class I
- Regulation number
- 872.3240
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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