Identity
- Trade Name
- Motility LAB-AGAR™ EUDAMED
- Device Name
- Motility LAB-AGAR™ EUDAMED
- Model / Reference
- PW 3023 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05902643939479 EUDAMED
- Basic UDI-DI
- 59026439ATMOTMS4 EUDAMED59026439ASMOTMRR EUDAMED
- EMDN Code
- W0104010206 MEDIA IN TUBES (SOLID & LIQUID) 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
Motility 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 | 59026439ATMOTMS4 | 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 acebd08d-0197-4669-9d19-a9428d00f50d 61 fields · synced Oct 6, 2026
- EUDAMED 2ac310ad-b6fe-42dc-a9f6-8341c6ffac3d 61 fields · synced Oct 6, 2026