Identity
- Trade Name
- XLD MEDIUM EUDAMED
- Device Name
- XLD MEDIUM EUDAMED
- Model / Reference
- PO0164A EUDAMEDCM0469W EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05032384018093 EUDAMED05032384510733 EUDAMED
- Basic UDI-DI
- 5032384XLDMediumPlate37 EUDAMED5032384XLDMediumOL7Q EUDAMED
- EMDN Code
- W0104010405 NON-CHROMOGENIC MEDIA (PLATES) EUDAMEDW0104010101 DEHYDRATED CULTURE MEDIA (DCM) EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
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
Xld Medium by Oxoid Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 5032384XLDMediumPlate37 | Class A | Active |
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Manufacturer
- Manufacturer
- Oxoid Ltd
- EUDAMED SRN
- GB-MF-000016914
- Authorised Representative
- Thermo Fisher Diagnostics B.V. NL-AR-000013157
Sources (2)
- EUDAMED 729eccac-9e08-4797-919f-0459deef0aaf 61 fields · synced Jul 29, 2026
- EUDAMED 73240080-e452-4108-a913-fc7f877d0f30 61 fields · synced May 19, 2026