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AFP screening IRMA KIT

EUDAMED

Class C (EU MDR)

Ref A37404Model Immunoassay A37404

by IMMUNOTECH s.r.o.

Identity

Trade Name
AFP screening IRMA KIT EUDAMED
Device Name
AFP screening IRMA KIT EUDAMED
Model / Reference
Immunoassay A37404 EUDAMED
A37404 EUDAMED

Identifiers

Primary DI / UDI-DI
15099590203139 EUDAMED
Basic UDI-DI
150995905A37404SN EUDAMED
EMDN Code
W0102050299 PREGNANCY TESTING HORMONES - OTHER EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

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

AFP screening IRMA KIT by IMMUNOTECH s.r.o. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
IMMUNOTECH s.r.o.
EUDAMED SRN
CZ-MF-000001761

Sources (1)

  • EUDAMED 7ea8eb76-b6fc-4b6c-a545-2bb5627f153a 61 fields · synced Jun 19, 2026