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Progesterone (Electrochemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref 697023Model 50TModel 50T, 2×50T, 100T, 2×100T

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Progesterone (Electrochemiluminescence Immunoassay) EUDAMED
Device Name
Progesterone (Electrochemiluminescence Immunoassay) EUDAMED
Model / Reference
50T EUDAMED
697023 EUDAMED
50T, 2×50T, 100T, 2×100T EUDAMED

Identifiers

Primary DI / UDI-DI
06970341686000 EUDAMED
Basic UDI-DI
B-06970341686000 EUDAMED
69703416803205030J4 EUDAMED
EMDN Code
W0102050106 PROGESTERONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Class B 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

New Device

No

EUDAMED

Progesterone (Electrochemiluminescence Immunoassay) by Shenzhen Lifotronic Technology Co., Ltd. — Class IVD General — IVDR, IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000005654
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED abc4b2e5-d807-4d3d-ba0e-ed32945416dc 61 fields · synced Jun 19, 2026
  • EUDAMED a14d3ee5-4a5d-41e4-9582-fd24812ba343 61 fields · synced May 19, 2026