PhysioSelect TCR 696993
by Candulor AG
PhysioSelect TCR 696993 is a Class II device made by Candulor AG, listed in FDA GUDID since 10 May 2021 (UDI-DI E1996969931), registry data as of 22 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 | NumberE1996969931 | Date10 May 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PhysioSelect TCR
- Generic name
- Resin artificial teeth
- Model / Ref / Catalog
- 696993
- Primary DI / UDI-DI
- E1996969931
- FDA product code
- ELM
- GMDN term
- Resin artificial teeth
- Device class
- Class II
- Regulation number
- 872.3590
- GUDID distribution status
- In Commercial Distribution
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