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Advanced Instruments Standard Anoxomat Jar, Small AJ9022

by Advanced Instruments, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816068020931 UDI-DI Date12 Jun 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  • Withdrawn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
Advanced Instruments Standard Anoxomat Jar, Small
Generic Name
Anaerobic (AnO2) atmospheric generation IVD
Model / Ref / Catalog
AJ9022
Primary DI / UDI-DI
00816068020931
FDA Product Code
KZJ
GMDN Term
Anaerobic (AnO2) atmospheric generation IVD
Device Class
Class I
Regulation Number
866.2580
GUDID distribution status
In Commercial Distribution

From the manufacturer

Manufacturer's product page: Anoxomat® III Anaerobic Jar System

Other devices from Advanced Instruments, LLC

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Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

  • 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No