Sinfony™ 49640
by 3M Deutschland GmbH 2 variants
Sinfony™ 49640 is a Class II device made by 3M Deutschland GmbH, listed in FDA GUDID since 4 Aug 2017 (UDI-DI 04035077000895), 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 | Number04035077000895 | Date4 Aug 2017 | StatusListed |
Official records
- AccessGUDID record 04035077000895
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Sinfony™
- Generic name
- Denture reliner, hard
- Model / Ref / Catalog
- 49640
- Primary DI / UDI-DI
- 04035077000895
- FDA product code
- EBF
- GMDN term
- Denture reliner, hard
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
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