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MutaPLATE® MTHFR™

EUDAMED

Class IVD General (EU MDR)

Ref KF1901432

by Immundiagnostik AG

Identity

Trade Name
MutaPLATE® MTHFR™ EUDAMED
Device Name
MutaPLATE® MTHFR™ EUDAMED
Model / Reference
KF1901432 EUDAMED

Identifiers

Primary DI / UDI-DI
04050598002692 EUDAMED
Basic UDI-DI
B-04050598002692 EUDAMED
EMDN Code
W0106010499 POLYMORPHISM TESTS - OTHER EUDAMED

Classification

Device Class
Class IVD General 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

MutaPLATE® MTHFR™ by Immundiagnostik AG — 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

Manufacturer
Immundiagnostik AG
EUDAMED SRN
DE-MF-000020905

Sources (1)

  • EUDAMED 312d1a92-9f1d-4b96-99e8-e3774598863a 61 fields · synced Jul 13, 2026