← Back to catalogue

RIA Progesterone

EUDAMED

Class B (EU MDR)

Ref IM1188Model Immunoassay IM1188

by IMMUNOTECH s.r.o.

Identity

Trade Name
RIA Progesterone EUDAMED
Device Name
RIA Progesterone EUDAMED
Model / Reference
Immunoassay IM1188 EUDAMED
IM1188 EUDAMED

Identifiers

Primary DI / UDI-DI
15099590213817 EUDAMED
Basic UDI-DI
150995905IM11885T EUDAMED
EMDN Code
W0102050106 PROGESTERONE 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 Progesterone 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 e3d3cf94-6c21-45bb-8817-6d056305bfe8 61 fields · synced Jun 18, 2026