← Back to catalogue

RIA Δ4-Androstenedione

EUDAMED

Class B (EU MDR)

Ref IM0674Model Immunoassay, IM0674

by IMMUNOTECH s.r.o.

Identity

Trade Name
RIA Δ4-Androstenedione EUDAMED
Device Name
RIA Δ4-Androstenedione EUDAMED
Model / Reference
Immunoassay, IM0674 EUDAMED
IM0674 EUDAMED

Identifiers

Primary DI / UDI-DI
15099590213015 EUDAMED
Basic UDI-DI
150995905IM067462 EUDAMED
EMDN Code
W0102050101 ANDROSTENEDIONE EUDAMED

Classification

Device Class
Class B 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

RIA Δ4-Androstenedione by IMMUNOTECH s.r.o. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 2211f4b2-c6aa-49f0-8af1-ef1e19fc21b4 61 fields · synced Aug 4, 2026