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Progesterone CLIA Kit (Chemiluminescence Immunoassay)

EUDAMED

Class B (EU MDR)

Ref F11702Model 100 tests/box

by Beijing Diagreat Biotechnologies Co., Ltd.

Identity

Trade Name
Progesterone CLIA Kit (Chemiluminescence Immunoassay) EUDAMED
Device Name
Progesterone CLIA Kit (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
100 tests/box EUDAMED
F11702 EUDAMED

Identifiers

Primary DI / UDI-DI
06942293590100 EUDAMED
Basic UDI-DI
697518250F117022F EUDAMED
Direct Marketing DI
06942293590100 EUDAMED
EMDN Code
W0102050106 PROGESTERONE EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy 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

New Device

Yes

EUDAMED

Progesterone CLIA Kit (Chemiluminescence Immunoassay) by Beijing Diagreat Biotechnologies Co., Ltd. — Class B — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000019511
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 46d37926-b76e-44c9-8f8a-af541545dfeb 61 fields · synced Jun 18, 2026