Identity
- Trade Name
- Airgas Healthcare FDA UDI
- Generic Name
- Anaerobic chamber FDA UDI
- Device Name
- Used to grow and sustain anaerobic, aerobic bacteria, or cultures in a biological incubator. FDA UDI
- Model / Reference
- Device Gas FDA UDI
- Description
- Used to grow and sustain anaerobic, aerobic bacteria, or cultures in a biological incubator. FDA UDI
Identifiers
- Catalog Number
- Biological Atmosphere FDA UDI
- Primary DI / UDI-DI
- 00819601020061 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
Airgas Healthcare by Airgas Usa Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Airgas Usa Llc
Sources (1)
- FDA UDI 8ed2faf4-bc57-49af-afd9-7693c64a41fa 36 fields · synced Jun 1, 2026