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Cystatin C Test Kit (Immunoturbidimetric Assay)

EUDAMED

Class B (EU MDR)

Ref /

by URIT Medical Electronic Co., Ltd.

Identity

Device Name
Cystatin C Test Kit (Immunoturbidimetric Assay) EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740733342 EUDAMED
06935740739351 EUDAMED
06935740713108 EUDAMED
Basic UDI-DI
69357407ICAS000030AP EUDAMED
EMDN Code
W0102019008 CYSTATIN C EUDAMED

Classification

Device Class
Class B 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

New Device

No

EUDAMED

Cystatin C Test Kit (Immunoturbidimetric Assay) by URIT Medical Electronic Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000011840
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (3)

  • EUDAMED 82669e12-5407-4b30-9c41-7e9e5ee4d284 61 fields · synced Oct 6, 2026
  • EUDAMED a8dfcb16-c7dd-488a-aa61-3bfc78bb9f8e 61 fields · synced May 17, 2026
  • EUDAMED 69cc0de3-d3df-4eef-9c06-63fa227f774a 61 fields · synced May 17, 2026