← Back to catalogue
Anaerogen Compact 10 Pack
EUDAMEDFDA UDIClass A (EU MDR)
Ref AN0020D
by Oxoid Ltd
Identity
- Trade Name
- ANAEROGEN COMPACT 10 PACK EUDAMEDANAEROGEN COMPACT FDA UDI
- Generic Name
- Atmospheric generation kit IVD FDA UDI
- Device Name
- ANAEROGEN EUDAMED
- Model / Reference
- AN0020D EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05032384446148 EUDAMEDFDA UDI
- Basic UDI-DI
- 5032384AnaerogenCompactSV EUDAMED
- FDA Product Code
- KZJ FDA UDI
- EMDN Code
- W0104010999 ENVIRONMENTAL GENERATING SYSTEMS - OTHER EUDAMED
- GMDN Term
- Atmospheric generation kit IVD FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass I FDA UDI
- Regulation Number
- 866.2580 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Anaerogen Compact 10 Pack by Oxoid Ltd — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 5032384AnaerogenCompactSV | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Oxoid Ltd
- EUDAMED SRN
- GB-MF-000016914
- Authorised Representative
- Thermo Fisher Diagnostics B.V. NL-AR-000013157
Sources (2)
- EUDAMED 7b21f4b9-be57-4304-8899-c2d94d1880df 61 fields · synced Jun 18, 2026
- FDA UDI 906ad852-7f4f-4483-9ea9-2358b9ab74cd 32 fields · synced May 30, 2026