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Angiotensin I RIA KIT

EUDAMED

Class B (EU MDR)

Ref IM3518Model Immunoassay, IM3518

by IMMUNOTECH s.r.o.

Identity

Trade Name
Angiotensin I RIA KIT EUDAMED
Device Name
Angiotensin I RIA KIT EUDAMED
Model / Reference
Immunoassay, IM3518 EUDAMED
IM3518 EUDAMED

Identifiers

Primary DI / UDI-DI
15099590219574 EUDAMED
Basic UDI-DI
150995905IM351868 EUDAMED
EMDN Code
W0102060202 ANGIOTENSIN I / II 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

Angiotensin I RIA 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 8ed2bc5f-9c63-4363-942f-6a59d8a17a04 61 fields · synced Jul 29, 2026