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Mighty Rest 12060310 230V

by Wheelchairs of Kansas

Mighty Rest 12060310 230V is a Class II device made by Wheelchairs of Kansas, listed in FDA GUDID since 8 May 2026 (UDI-DI 00845699003822), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845699003822 UDI-DI Date8 May 2026ListedStatusListed 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  • Withdrawn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

Trade name
Mighty Rest
Generic name
Bariatric bed
Model / reference
12060310 230V
Primary DI / UDI-DI
00845699003822
FDA product code
FNL
GMDN term
Bariatric bed
Device class
Class II
Regulation number
880.5100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital).

Other devices from Wheelchairs of Kansas

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)