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Amron Oxygen Treatment Hood 8891-03

by Amron International, Inc.

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 Number00860010778616 UDI-DI Date30 Dec 2024ListedStatusListed 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  • Withdrawn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
Amron Oxygen Treatment Hood
Generic Name
Oxygen administration hood, adult
Model / Reference
8891-03
Primary DI / UDI-DI
00860010778616
FDA Product Code
FOG
GMDN Term
Oxygen administration hood, adult
Device Class
Class I
Regulation Number
868.5700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Oxygen administration hood, adult

Other devices from Amron International, Inc.

Properties

  • Lot / Batch Number
  • Expiration Date
  • 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
  • Premarket Exempt: No
  • Serial Number: No