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IRT Neonatal Luminescence Immunoassay

EUDAMED

Class IVD General (EU MDR)

Ref RE68019

by IBL International GmbH

Identity

Trade Name
IRT Neonatal Luminescence Immunoassay EUDAMED
Device Name
IRT Neonatal Luminescence Immunoassay EUDAMED
Model / Reference
RE68019 EUDAMED

Identifiers

Primary DI / UDI-DI
04049325007666 EUDAMED
Basic UDI-DI
B-04049325007666 EUDAMED
EMDN Code
W0102019007 IMMUNO REACTIVE TRYPSIN 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

IRT Neonatal Luminescence Immunoassay 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 7f42aff2-7cc8-46d8-b232-f0e1eea112d2 61 fields · synced Jun 19, 2026