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Irma Igf-I

EUDAMED

Class B (EU MDR)

Ref A15729Model Immunoassay A15729

by IMMUNOTECH s.r.o.

Identity

Trade Name
IRMA IGF-I EUDAMED
Device Name
IRMA IGF-I EUDAMED
Model / Reference
Immunoassay A15729 EUDAMED
A15729 EUDAMED

Identifiers

Primary DI / UDI-DI
15099590201777 EUDAMED
Basic UDI-DI
150995905A15729SH EUDAMED
EMDN Code
W0102060403 INSULIN-LIKE GROWTH FACTOR I (SOMATOMEDIN C) 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

Irma Igf-I 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 b9065276-4e9e-491f-a6fc-e3033217a9f5 61 fields · synced Jun 19, 2026