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Cystatin C Determination Kit (Fluorescence Immunochromatographic Assay)

EUDAMED

Class B (EU MDR)

Ref P11001Model 25 tests

by Beijing Diagreat Biotechnologies Co., Ltd.

Identity

Trade Name
Cystatin C Determination Kit (Fluorescence Immunochromatographic Assay) EUDAMED
Device Name
Cystatin C Determination Kit (Fluorescence Immunochromatographic Assay) EUDAMED
Model / Reference
25 tests EUDAMED
P11001 EUDAMED

Identifiers

Primary DI / UDI-DI
06975182500218 EUDAMED
Basic UDI-DI
697518250P110015C EUDAMED
Direct Marketing DI
06975182500218 EUDAMED
EMDN Code
W0102019008 CYSTATIN C EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

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

Cystatin C Determination Kit (Fluorescence Immunochromatographic Assay) 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 ba2abe08-cbd9-43cd-8e6a-a8548b58a583 61 fields · synced Jun 18, 2026