Identity
- Trade Name
- MRS LAB-AGAR™ EUDAMED
- Device Name
- MRS LAB-AGAR™ EUDAMED
- Model / Reference
- BT 5031.02 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05902643947399 EUDAMED
- Basic UDI-DI
- 59026439ABMRSLG EUDAMED59026439ASMRSQ7 EUDAMED
- EMDN Code
- W0104010306 CULTURE MEDIA IN BOTTLES EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
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
Mrs 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 | 59026439ABMRSLG | Class A | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BioMaxima Spółka Akcyjna
- EUDAMED SRN
- PL-MF-000039473
Sources (2)
- EUDAMED e7d8673b-3108-4974-968e-46775e74a0d6 61 fields · synced Jun 19, 2026
- EUDAMED 07a4cfe0-37dc-4b13-8910-0ac229d0a3c6 61 fields · synced Jun 19, 2026