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Quickie 200R

by Sunrise Medical (US) LLC

Quickie 200R (EIPW35) is a wheelchair recliner (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Sunrise Medical (US) LLC, listed in FDA GUDID since 5 Sep 2023 (UDI-DI 00016958058680), registry data as of 16 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 16 Oct 2026.

Regulatory status

as of registry sync 16 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00016958058680 UDI-DI Date5 Sep 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Wheelchair recliner, battery-powered
Model / Ref / Catalog
200R, EIPW35
Primary DI / UDI-DI
00016958058680
FDA product code
ITI
GMDN term
Wheelchair recliner, battery-powered
Device class
Class II
Regulation number
890.3860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wheelchair recliner, battery-powered

Similar devices

Other devices filed under FDA product code ITI (Wheelchair, Powered).

Other devices from Sunrise Medical (US) LLC

See all devices from Sunrise Medical (US) LLC →

Properties

  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)