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Aspartate Aminotransferase Reagent Kit (Aspartic Acid Substrate Method)

EUDAMED

Class B (EU MDR)

Ref /

by URIT Medical Electronic Co., Ltd.

Identity

Device Name
Aspartate Aminotransferase Reagent Kit (Aspartic Acid Substrate Method) EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740740746 EUDAMED
Basic UDI-DI
69357407ICAS000017AX EUDAMED
EMDN Code
W01010110 ASPARTATE AMINO-TRANSFERASE 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: Total aspartate aminotransferase (AST) IVD, reagent

Aspartate Aminotransferase Reagent Kit (Aspartic Acid Substrate Method) by URIT Medical Electronic Co., Ltd. — Class B — IVDR — listed in EUDAMED

Similar devices

Also classified as Total aspartate aminotransferase (AST) 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 (1)

  • EUDAMED d6edd809-dfd2-4cf6-82ea-351d7565061a 61 fields · synced Jun 18, 2026