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Uric Acid Reagent Kit (Uricase-Peroxidase Method)

EUDAMED

Class B (EU MDR)

Ref /

by URIT Medical Electronic Co., Ltd.

Identity

Device Name
Uric Acid Reagent Kit (Uricase-Peroxidase Method) EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740733328 EUDAMED
06935740740807 EUDAMED
Basic UDI-DI
69357407ICAS000020AL EUDAMED
EMDN Code
W01010232 URIC ACID 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

Category: Uric acid IVD, reagent

Uric Acid Reagent Kit (Uricase-Peroxidase Method) by URIT Medical Electronic Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, reagent.

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 (2)

  • EUDAMED 6446c296-1ca4-4327-a8f1-37d493c898e3 61 fields · synced Jul 30, 2026
  • EUDAMED 66b33f6b-da2b-4edf-aabe-c94a895c771f 61 fields · synced May 18, 2026