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E2 Detection Kit (Immunofluorescence Chromatography)

EUDAMED

Class IVD General (EU MDR)

Ref GKPD175

by Dezhou Guoke Medical Technology Co., Ltd.

Identity

Trade Name
E2 Detection Kit (Immunofluorescence Chromatography) EUDAMED
Device Name
E2 Detection Kit (Immunofluorescence Chromatography) EUDAMED
Model / Reference
GKPD175 EUDAMED

Identifiers

Primary DI / UDI-DI
D-GKPD175XV EUDAMED
Basic UDI-DI
B-GKPD175XV EUDAMED
EMDN Code
W0102050103 ESTRADIOL EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

E2 Detection Kit (Immunofluorescence Chromatography) by Dezhou Guoke Medical Technology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000044128
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED eae4165a-173e-44be-a8c0-71419b667073 61 fields · synced Jun 19, 2026