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Citadel Plus FX811B3B4AMABB

by Arjohuntleigh AB

Citadel Plus FX811B3B4AMABB is a Class II device made by Arjohuntleigh AB, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 05055982756532), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05055982756532 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Citadel Plus
Generic name
Bariatric bed
Model / reference
FX811B3B4AMABB
Primary DI / UDI-DI
05055982756532
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 Arjohuntleigh AB

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Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)