Footboard 12913-MH
Footboard 12913-MH is a Class II device made by Dynarex Corp., listed in FDA GUDID since 8 Feb 2021 (UDI-DI 00840117303119), 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 | Number00840117303119 | Date8 Feb 2021 | StatusListed |
Official records
- AccessGUDID record 00840117303119
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Footboard
- Generic name
- Basic electric home bed
- Model / reference
- 12913-MH
- Primary DI / UDI-DI
- 00840117303119
- FDA product code
- FNL
- GMDN term
- Basic electric home bed
- Device class
- Class II
- Regulation number
- 880.5100
- GUDID distribution status
- In Commercial Distribution
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