TP001
Part of a family of 22 devices: see the family page
Ref TP001
TP001 is a Class I device made by ZimVie US Corp LLC, registered in EUDAMED on 5 Jun 2026 (Basic UDI-DI 844868A1GS) and listed in FDA GUDID since 24 Mar 2016 (UDI-DI 00844868017127), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number844868A1GS 00844868017127 | Date5 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00844868017127 | Date24 Mar 2016 | StatusListed |
Official records
- EUDAMED public site 844868A1GS
- AccessGUDID record 00844868017127
Across registries
- EUDAMED Basic UDI-DI 844868A1GS registered 5 Jun 2026 Active
- FDA GUDID UDI-DI 00844868017127 listed 24 Mar 2016 Listed
Timeline
- Listed FDA GUDID 00844868017127
- Registered EUDAMED 844868A1GS
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Dental soft-tissue coring punch, reusable
- Device name
- Reusable Surgical Dental Instruments
- Model / reference
- TP001
- Primary DI / UDI-DI
- 00844868017127
- Basic UDI-DI
- 844868A1GS
- FDA product code
- NDP
- EMDN code
- L159099 Odontostomatology instruments, reusable - other
- GMDN term
- Dental soft-tissue coring punch, reusable
- Device class
- Class I
- Regulation number
- 872.3980
- EU registration type
- Standard device
- EU market of registration
- Spain
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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