← Back to catalogue

Advanced Instruments Ergonomic Culture Jar, Small

FDA UDI

Class I (US FDA UDI)

by Advanced Instruments, LLC

Identity

Trade Name
Advanced Instruments Ergonomic Culture Jar, Small FDA UDI
Generic Name
Anaerobic (AnO2) atmospheric generation IVD FDA UDI
Device Name
The Advanced Instruments ergonomic anaerobic jars provide flexibility and ease-of-use for laboratory technicians while maximizing incubator and laboratory space. All Anoxomat jars are built to meet the highest microbiological and mechanical standards and minimize the risk of oxygen leaks. The small jar has a capacity of 12 petri dishes. FDA UDI
Model / Reference
AJ9049 FDA UDI
Description
The Advanced Instruments ergonomic anaerobic jars provide flexibility and ease-of-use for laboratory technicians while maximizing incubator and laboratory space. All Anoxomat jars are built to meet the highest microbiological and mechanical standards and minimize the risk of oxygen leaks. The small jar has a capacity of 12 petri dishes. FDA UDI

Identifiers

Catalog Number
AJ9049 FDA UDI
Primary DI / UDI-DI
00816068020917 FDA UDI
FDA Product Code
KZJ FDA UDI
GMDN Term
Anaerobic (AnO2) atmospheric generation IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaerobic (AnO2) atmospheric generation IVD

Advanced Instruments Ergonomic Culture Jar, Small by Advanced Instruments, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaerobic (AnO2) atmospheric generation IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0dc023dd-67f8-4324-a5b4-ae5b0c38c154 35 fields · synced Jun 8, 2026