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Progesterone Detection Kit (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref 3008722Model 100Tests/KitRef 3013916Model 2×50Tests/Kit

by Dirui Industrial Co., Ltd

Identity

Trade Name
Progesterone Detection Kit (Chemiluminescence Immunoassay) EUDAMED
Device Name
Progesterone Detection Kit (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
100Tests/Kit EUDAMED
3008722 EUDAMED
2×50Tests/Kit EUDAMED
3013916 EUDAMED

Identifiers

Primary DI / UDI-DI
06925794511751 EUDAMED
06942202224102 EUDAMED
Basic UDI-DI
B-06925794511751 EUDAMED
B-06942202224102 EUDAMED
EMDN Code
W0102050106 PROGESTERONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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

Progesterone Detection Kit (Chemiluminescence Immunoassay) by Dirui Industrial 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-000001891
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 22d25687-8a38-41c1-b67b-3827d9cdb064 61 fields · synced Aug 3, 2026
  • EUDAMED 34b86dc6-2ab3-4810-ac48-497e2388f4a4 61 fields · synced May 18, 2026