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Progesterone (Prog)Test Kit (Homogeneous Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref HCLIA15111

by Nanjing Poclight Biotechnology Co., Ltd.

Identity

Trade Name
Progesterone (Prog)Test Kit (Homogeneous Chemiluminescence Immunoassay) EUDAMED
Device Name
Progesterone (Prog)Test Kit (Homogeneous Chemiluminescence Immunoassay) EUDAMED
Model / Reference
HCLIA15111 EUDAMED

Identifiers

Primary DI / UDI-DI
06974524061738 EUDAMED
Basic UDI-DI
B-06974524061738 EUDAMED
EMDN Code
W0102050106 PROGESTERONE 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

Progesterone (Prog)Test Kit (Homogeneous Chemiluminescence Immunoassay) by Nanjing Poclight Biotechnology Co., Ltd. — Class IVD General — IVDD — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000039609
Authorised Representative
HUMISS TRADING S. L. ES-AR-000040177

Sources (1)

  • EUDAMED 864a5795-5dc3-4499-a4b1-f85cd1c14081 61 fields · synced Oct 8, 2026