# Merits P326A0M-Armub

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/merits-p326a0m-armub>
- Manufacturer: [Merits Health Products., Inc.](https://devicerts.com/manufacturers/fda-fei-1000221992) (FDA registration: Taiwan)
- Name in the registry: MERITS P326A0M-ARMUB
- Device class: Class II (US FDA)
- FDA product code: ITI
- GMDN: Wheelchair, power-assisted, occupant-controlled, non-collapsible (38529)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 04714379297638 · listed 2023-02-28 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K012802 · decision 2001-09-18 · decision SESE · status: Active · from GUDID

## Recalls

- Z-1504-2021 · Class II · ongoing · initiated 2021-04-01: Seat baseplate pin has broken in the field.

## Identity

- Trade name: MERITS [FDA GUDID (AccessGUDID)]
- Generic name: Wheelchair, power-assisted, occupant-controlled, non-collapsible [FDA GUDID (AccessGUDID)]
- Model / reference: P326A0M-ARMUB [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 04714379297638 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K012802 [FDA GUDID (AccessGUDID)]
- FDA product code: ITI [FDA GUDID (AccessGUDID)]
- GMDN term: Wheelchair, power-assisted, occupant-controlled, non-collapsible (38529) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 890.3860 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Prescription use: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Merits P326A0M-Armub, Merits Health Products., Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/merits-p326a0m-armub (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/merits-p326a0m-armub.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/merits-p326a0m-armub
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.