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CysC Fast Test Kit (Immunofluorescence Assay)

EUDAMED

Class IVD General (EU MDR)

Ref /Ref IF5008

by Getein Biotech, Inc.

Identity

Trade Name
CysC Fast Test Kit (Immunofluorescence Assay) EUDAMED
Device Name
CysC Fast Test Kit (Immunofluorescence Assay) EUDAMED
Model / Reference
/ EUDAMED
IF5008 EUDAMED

Identifiers

Primary DI / UDI-DI
06954414702101 EUDAMED
06954414792676 EUDAMED
Basic UDI-DI
B-06954414702101 EUDAMED
695441470210GR EUDAMED
EMDN Code
W0102019008 CYSTATIN C EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Class B EUDAMED
Market of Registration
Netherlands EUDAMED
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMEDEUDAMED

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

CysC Fast Test Kit (Immunofluorescence Assay) by Getein Biotech, Inc. — Class IVD General — IVDR, IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000017986
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (2)

  • EUDAMED 30026a9f-6039-4d3f-ab02-0a28e801431f 61 fields · synced Jul 26, 2026
  • EUDAMED 32df2186-7cfd-444c-954f-8bc5573f55ac 61 fields · synced Jul 26, 2026