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Neopterin ELISA

EUDAMED

Class B (EU MDR)

Ref RE59321

by IBL International GmbH

Identity

Trade Name
Neopterin ELISA EUDAMED
Device Name
Neopterin ELISA EUDAMED
Model / Reference
RE59321 EUDAMED

Identifiers

Primary DI / UDI-DI
04049325030664 EUDAMED
Basic UDI-DI
4049325IVR05060001BS2 EUDAMED
Direct Marketing DI
04049325030664 EUDAMED
EMDN Code
W0102069004 NEOPTERINE EUDAMED

Classification

Device Class
Class B 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

New Device

No

EUDAMED

Neopterin ELISA by Ibl International Gmbh — 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

EUDAMED SRN
DE-MF-000015709

Sources (1)

  • EUDAMED 8b98b4b8-25a8-4564-8b5c-caa639471f14 61 fields · synced Jun 18, 2026