← Back to catalogue
Sorbitol Macconkey Agar
EUDAMEDFDA UDIClass A (EU MDR)
Ref CM0813B
by Oxoid Ltd
Identity
- Trade Name
- SORBITOL MACCONKEY AGAR EUDAMEDFDA UDI
- Generic Name
- Differential/selective agar culture medium IVD FDA UDI
- Device Name
- SORBITOL MACCONKEY AGAR EUDAMED
- Model / Reference
- CM0813B EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05032384004072 EUDAMEDFDA UDI
- Basic UDI-DI
- 5032384SorbMacConkOLSY EUDAMED
- 510(k) Number
- K872956 FDA UDI
- FDA Product Code
- JSI FDA UDI
- EMDN Code
- W0104010101 DEHYDRATED CULTURE MEDIA (DCM) 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
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Sorbitol Macconkey Agar 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 | 5032384SorbMacConkOLSY | 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 f94b194c-f2ee-4ab6-9831-8e30a20001e9 61 fields · synced Jul 11, 2026
- FDA UDI d6e43448-1b24-47c1-ae37-2f31ab83bbc6 33 fields · synced May 30, 2026