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Progesterone (Prog) Test Kit (Immunofluorescence)

EUDAMED

Class IVD General (EU MDR)

Ref 52027109Model 50T/Kit

by Genrui Biotech Inc.

Identity

Trade Name
Progesterone (Prog) Test Kit (Immunofluorescence) EUDAMED
Device Name
Progesterone (Prog) Test Kit (Immunofluorescence) EUDAMED
Model / Reference
50T/Kit EUDAMED
52027109 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FA0023Z4 EUDAMED
Basic UDI-DI
B-FA0023Z4 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 (Immunofluorescence) by Genrui Biotech Inc. — 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
Genrui Biotech Inc.
EUDAMED SRN
CN-MF-000017351
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED d65ba231-79ff-4d50-82ec-643f4ff9ae7e 61 fields · synced Jun 19, 2026