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C-Reactive Protein/Anti-streptolysin O/Rheumatoid Factor Reagent Kit

EUDAMED

Class IVD General (EU MDR)

Ref 2U001

by Changsha Sinocare Inc.

Identity

Device Name
C-Reactive Protein/Anti-streptolysin O/Rheumatoid Factor Reagent Kit EUDAMED
Model / Reference
2U001 EUDAMED

Identifiers

Primary DI / UDI-DI
D-02B0029YZ EUDAMED
Basic UDI-DI
B-02B0029YZ EUDAMED
EMDN Code
W01021104,W01021109,W01021110 EUDAMED

Classification

Device Class
Class IVD General 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

C-Reactive Protein/Anti-streptolysin O/Rheumatoid Factor 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 bb3d92ab-ca95-44eb-849f-85f175fef655 61 fields · synced Aug 1, 2026