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selenOtest ELISA

EUDAMED

Class B (EU MDR)

Ref YC5900

by Immundiagnostik AG

Identity

Trade Name
selenOtest ELISA EUDAMED
Device Name
selenOtest ELISA EUDAMED
Model / Reference
YC5900 EUDAMED

Identifiers

Primary DI / UDI-DI
04050598014619 EUDAMED
Basic UDI-DI
4050598MNTRELXY EUDAMED
Direct Marketing DI
04050598014619 EUDAMED
EMDN Code
W0102010399 TRANSPORT PROTEINS - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

selenOtest ELISA by Immundiagnostik AG — 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
Immundiagnostik AG
EUDAMED SRN
DE-MF-000020905

Sources (1)

  • EUDAMED 14227e20-4815-4d96-974f-bc471292fce2 61 fields · synced Jul 16, 2026