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Aldosterone ELISA

EUDAMED

Class IVD General (EU MDR)

Ref RE52301

by IBL International GmbH

Identity

Trade Name
Aldosterone ELISA EUDAMED
Device Name
Aldosterone ELISA EUDAMED
Model / Reference
RE52301 EUDAMED

Identifiers

Primary DI / UDI-DI
04049325007512 EUDAMED
Basic UDI-DI
B-04049325007512 EUDAMED
EMDN Code
W0102060201 ALDOSTERONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

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

Aldosterone ELISA by Ibl International Gmbh — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
DE-MF-000015709

Sources (1)

  • EUDAMED 0a46d1ed-84d4-4a43-94aa-6965df3a3a2d 61 fields · synced Jul 18, 2026