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Anaerobic Artificial Atmosphere

FDA UDI

Class I (US FDA UDI)

by Oxarc, LLC

Identity

Trade Name
Anaerobic Artificial Atmosphere FDA UDI
Generic Name
Anaerobic chamber FDA UDI
Device Name
GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Anaerobic Artificial Atmosphere FDA UDI
Model / Reference
1 FDA UDI
Description
GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Anaerobic Artificial Atmosphere FDA UDI

Identifiers

Primary DI / UDI-DI
00860009626218 FDA UDI
FDA Product Code
BXK FDA UDI
GMDN Term
Anaerobic chamber FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaerobic chamber

Anaerobic Artificial Atmosphere by Oxarc, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaerobic chamber.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oxarc, LLC

Sources (1)

  • FDA UDI f43a3969-87e5-4acc-8b4f-7f0f25a3cee7 33 fields · synced May 30, 2026