DS PrimeTaper 68017291
by Dentsply Implants Manufacturing GmbH
DS PrimeTaper 68017291 is a Class I device made by Dentsply Implants Manufacturing GmbH, listed in FDA GUDID since 3 Jun 2024 (UDI-DI 07392532279645), 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 | Number07392532279645 | Date3 Jun 2024 | StatusListed |
Official records
- AccessGUDID record 07392532279645
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- DS PrimeTaper
- Generic name
- Surgical drill guide, single-use
- Model / Ref / Catalog
- 68017291
- Primary DI / UDI-DI
- 07392532279645
- FDA product code
- NDP
- GMDN term
- Surgical drill guide, single-use
- Device class
- Class I
- Regulation number
- 872.3980
- GUDID distribution status
- In Commercial Distribution
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