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Neonatal IRT FEIA

EUDAMED

Class IVD General (EU MDR)

Ref 6199831

by Labsystems Diagnostics Oy

Identity

Trade Name
Neonatal IRT FEIA EUDAMED
Device Name
Neonatal IRT FEIA EUDAMED
Model / Reference
6199831 EUDAMED

Identifiers

Primary DI / UDI-DI
06438172214026 EUDAMED
Basic UDI-DI
B-06438172214026 EUDAMED
EMDN Code
W01010199 ENZYMES - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Neonatal IRT FEIA by Labsystems Diagnostics Oy — 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
FI-MF-000018281

Sources (1)

  • EUDAMED da21c75d-ccdd-4ed3-b771-415d63b505ae 61 fields · synced Jun 17, 2026