Identity
- Trade Name
- Mueller Hinton 2 LAB-AGAR™ EUDAMED
- Device Name
- Mueller Hinton 2 LAB-AGAR™ EUDAMED
- Model / Reference
- PPK 0016 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05902643932036 EUDAMED
- Basic UDI-DI
- 59026439ASMHR6 EUDAMED
- EMDN Code
- W0104010405 NON-CHROMOGENIC MEDIA (PLATES) EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
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
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Mueller Hinton 2 LAB-AGAR™ by BioMaxima Spółka Akcyjna — 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 | 59026439ASMHR6 | Class A | Active |
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Manufacturer
- Manufacturer
- BioMaxima Spółka Akcyjna
- EUDAMED SRN
- PL-MF-000039473
Sources (1)
- EUDAMED 7a0ea9d9-d93e-492c-8e28-9c26bbb7dae0 61 fields · synced Jun 18, 2026