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Lh Irma Kit

EUDAMED

Class B (EU MDR)

Ref IM3302Model Immunoassay IM1381, IM3302

by IMMUNOTECH s.r.o.

Identity

Trade Name
LH IRMA KIT EUDAMED
Device Name
LH IRMA KIT EUDAMED
Model / Reference
Immunoassay IM1381, IM3302 EUDAMED
IM3302 EUDAMED

Identifiers

Primary DI / UDI-DI
15099590218911 EUDAMED
Basic UDI-DI
150995905LHIRMAHQ EUDAMED
EMDN Code
W0102050105 LUTEINISING HORMONE 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

Lh Irma Kit 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

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Manufacturer

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

Sources (1)

  • EUDAMED a80e12ed-f74d-4e24-8efa-431db12eea8f 61 fields · synced Jun 18, 2026