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Aircast 31M-900

by Djo, LLC

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00190446979128 UDI-DI Date3 Aug 2026ListedStatusListed 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  • Withdrawn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
Aircast
Generic name
Multi-chamber venous compression system garment, reusable
Model / reference
31M-900
Primary DI / UDI-DI
00190446979128
FDA product code
JOW
GMDN term
Multi-chamber venous compression system garment, reusable
Device class
Class II
Regulation number
870.5800
GUDID distribution status
In Commercial Distribution

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

  • Prescription use
  • Lot / batch number

Other properties (13)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No