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α1-Microglobulin (α1-MG) testing kit (Latex Immunoturbidimetric Assay)

EUDAMED

Class B (EU MDR)

Ref /

by URIT Medical Electronic Co., Ltd.

Identity

Device Name
α1-Microglobulin (α1-MG) testing kit (Latex Immunoturbidimetric Assay) EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740733373 EUDAMED
Basic UDI-DI
69357407ICAS000033AV EUDAMED
EMDN Code
W0102019004 A1-MICROGLOBULIN 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

α1-Microglobulin (α1-MG) testing kit (Latex Immunoturbidimetric Assay) by URIT Medical Electronic 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-000011840
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 75cc62f1-37ae-4377-9d18-30591a6abc87 61 fields · synced Jun 19, 2026