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FSH / LH Detection Kit (Immunofluorescence Chromatography)

EUDAMED

Class IVD General (EU MDR)

Ref GKPD172

by Dezhou Guoke Medical Technology Co., Ltd.

Identity

Trade Name
FSH / LH Detection Kit (Immunofluorescence Chromatography) EUDAMED
Device Name
FSH / LH Detection Kit (Immunofluorescence Chromatography) EUDAMED
Model / Reference
GKPD172 EUDAMED

Identifiers

Primary DI / UDI-DI
D-GKPD172XP EUDAMED
Basic UDI-DI
B-GKPD172XP EUDAMED
EMDN Code
W0102160399 FERTILITY/PREGNANCY RT & POC - 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

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

FSH / LH 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 18327beb-7f19-46dc-96ea-cb39a12971da 61 fields · synced Jul 26, 2026