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Glucose/Homocysteine/Uric Acid/Low Density Lipoprotein Cholesterol Reagent Kit

EUDAMED

Class IVD General (EU MDR)

Ref 1Q001

by Changsha Sinocare Inc.

Identity

Device Name
Glucose/Homocysteine/Uric Acid/Low Density Lipoprotein Cholesterol Reagent Kit EUDAMED
Model / Reference
1Q001 EUDAMED

Identifiers

Primary DI / UDI-DI
D-02B0001YB EUDAMED
Basic UDI-DI
B-02B0001YB EUDAMED
EMDN Code
W01010213,W01010221,W01010232,W01021307 EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Glucose/Homocysteine/Uric Acid/Low Density Lipoprotein Cholesterol Reagent Kit by Changsha Sinocare Inc. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000012244
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 87519649-b821-421e-8cbc-a4956725b7f7 61 fields · synced Jul 26, 2026