Identity
- Trade Name
- PRAS CAMPY EUDAMEDPRAS Campylobacter Selective Agar (CAMPY) FDA UDI
- Generic Name
- Differential/selective agar culture medium IVD FDA UDI
- Device Name
- Anaerobic Culture Media EUDAMEDAS-211 Campylobacter Selective Agar (CAMPY) is used for the selective isolation of Campylobacter jejuni subsp. jejuni from fecal or rectal swabs. Pre-reduced anaerobically sterilized (PRAS). 100 x 15 mm agar plate. Transparent red. 1 plate per pack. FDA UDI
- Model / Reference
- AS-211 EUDAMEDFDA UDI
- Description
- AS-211 Campylobacter Selective Agar (CAMPY) is used for the selective isolation of Campylobacter jejuni subsp. jejuni from fecal or rectal swabs. Pre-reduced anaerobically sterilized (PRAS). 100 x 15 mm agar plate. Transparent red. 1 plate per pack. FDA UDI
Identifiers
- Catalog Number
- AS-211 FDA UDI
- Primary DI / UDI-DI
- 00810048900091 EUDAMEDFDA UDI
- Basic UDI-DI
- 081004890ANAEROBEDT EUDAMED
- FDA Product Code
- JSJ FDA UDI
- EMDN Code
- W0104010405 NON-CHROMOGENIC MEDIA (PLATES) EUDAMED
- GMDN Term
- Differential/selective agar culture medium IVD FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass I FDA UDI
- Regulation Number
- 866.2360 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
No
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
Pras Campy by Anaerobe Systems — 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 | 081004890ANAEROBEDT | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
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Manufacturer
- Manufacturer
- Anaerobe Systems
- EUDAMED SRN
- US-MF-000040030
- Authorised Representative
- Casus Europe B.V. NL-AR-000037688
Sources (2)
- EUDAMED a92491a9-7aa2-4dc1-b33c-a7d4b6d86820 61 fields · synced Jul 29, 2026
- FDA UDI 82b52efb-24e3-4b53-92bd-f3e07346f3e4 36 fields · synced May 30, 2026