Dmi 522-1816-1999
Dmi 522-1816-1999 is a Class I device made by Dms Holdings, Inc.,, listed in FDA GUDID since 23 Jun 2023 (UDI-DI 00041298524113), 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 | Number00041298524113 | Date23 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 00041298524113
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dmi
- Generic name
- Bath back rest/seat
- Model / reference
- 522-1816-1999
- Primary DI / UDI-DI
- 00041298524113
- FDA product code
- ILS
- GMDN term
- Bath back rest/seat
- Device class
- Class I
- Regulation number
- 890.5050
- GUDID distribution status
- In Commercial Distribution
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