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Hercules Air Mattress Controller Controller, Kap Medical, Revision A

by Morel Company, LLC., the

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00819552022343 UDI-DI Date17 Dec 2025ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Hercules Air Mattress Controller
Generic Name
Basic electric hospital bed
Model / Ref / Catalog
Controller, Kap Medical, Revision A, CKA
Primary DI / UDI-DI
00819552022343
FDA Product Code
FNL
GMDN Term
Basic electric hospital bed
Device Class
Class II
Regulation Number
880.5100
GUDID distribution status
Not in Commercial Distribution

Other devices from The Morel Company

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Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No