Merits P326DMBBMUB
by Merits Health Products., Inc.
Merits P326DMBBMUB is an electric-motor-driven wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Merits Health Products., Inc., cleared under FDA 510(k) K012802 on 18 Sep 2001 and listed in FDA GUDID since 21 Oct 2026 (UDI-DI 04714379299717), active as of 2 Nov 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04714379299717 | Date21 Oct 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK012802 | Date18 Sep 2001 | StatusActive |
Official records
- AccessGUDID record 04714379299717
- FDA 510(k) database K012802
Across registries
- FDA 510(k) K012802 decided 18 Sep 2001 Active
- FDA GUDID UDI-DI 04714379299717 listed 21 Oct 2026 Listed
Recalls
-
- Ongoing Z-1504-2021
Seat baseplate pin has broken in the field.
Timeline
- Cleared FDA 510(k) K012802
- Recall initiated FDA recalls Z-1504-2021
- Listed FDA GUDID 04714379299717
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Merits
- Generic name
- Electric-motor-driven wheelchair, occupant-controlled
- Model / reference
- P326DMBBMUB
- Primary DI / UDI-DI
- 04714379299717
- 510(k) Number
- FDA product code
- ITI
- GMDN term
- Electric-motor-driven wheelchair, occupant-controlled
- Device class
- Class II
- Regulation number
- 890.3860
- GUDID distribution status
- In Commercial Distribution
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