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K-4oem AIRE-FLOAT MATRIX-ALALMS8

by Kap Medical

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817012031805 UDI-DI Date1 Oct 2025ListedStatusListed GUDID: 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  • Withdrawn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
K-4oem AIRE-FLOAT
Generic Name
Low-air-loss bed
Model / Ref / Catalog
MATRIX-ALALMS8
Primary DI / UDI-DI
00817012031805
FDA Product Code
FNM
GMDN Term
Low-air-loss bed
Device Class
Class II
Regulation Number
880.5550
GUDID distribution status
In Commercial Distribution

Other devices from Kap Medical

See all devices from Kap Medical →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No