Identity
- Trade Name
- PRAS BBE/LKV EUDAMEDPRAS BBE/LKV Biplate FDA UDI
- Generic Name
- Multiple formulation agar culture medium IVD FDA UDI
- Device Name
- Anaerobic Culture Media EUDAMEDAS-212 BBE/LKV Bacteroides Bile Esculin (BBE) agar is an enriched, selective, and differential medium used for the isolation and presumptive identification of obligately anaerobic gram-negative bacilli of the Bacteroides fragilis group and Bilophila wadsworthia. Laked Brucella Blood Agar with Kanamycin and Vancomycin (LKV) is an enriched, selective, and differential medium for the isolation and partial identification of obligately anaerobic gram-negative bacilli. Pre-reduced anaerobically sterilized (PRAS). 100 x 15 mm split plate. BBE is transparent yellow/green. LKV is transparent red. 1 plate FDA UDI
- Model / Reference
- AS-212 EUDAMEDFDA UDI
- Description
- AS-212 BBE/LKV Bacteroides Bile Esculin (BBE) agar is an enriched, selective, and differential medium used for the isolation and presumptive identification of obligately anaerobic gram-negative bacilli of the Bacteroides fragilis group and Bilophila wadsworthia. Laked Brucella Blood Agar with Kanamycin and Vancomycin (LKV) is an enriched, selective, and differential medium for the isolation and partial identification of obligately anaerobic gram-negative bacilli. Pre-reduced anaerobically sterilized (PRAS). 100 x 15 mm split plate. BBE is transparent yellow/green. LKV is transparent red. 1 plate FDA UDI
Identifiers
- Catalog Number
- AS-212 FDA UDI
- Primary DI / UDI-DI
- 00810048900107 EUDAMEDFDA UDI
- Basic UDI-DI
- 081004890ANAEROBEDT EUDAMED
- FDA Product Code
- JSI FDA UDI
- EMDN Code
- W0104010405 NON-CHROMOGENIC MEDIA (PLATES) EUDAMED
- GMDN Term
- Multiple formulation 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 Bbe/Lkv 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 6a833d5c-9f72-466c-a3d7-29bbc7278d9d 61 fields · synced Jul 11, 2026
- FDA UDI c37377c7-3f50-4b37-8fcc-f717b9f7301a 36 fields · synced May 30, 2026