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C-Reactive Protein Test (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref 5M13C2-25-EU, 5M13C2-50-EU

by Xiamen Boson Biotech Co., Ltd.

Identity

Trade Name
C-Reactive Protein Test (FIA) EUDAMED
Device Name
C-Reactive Protein Test (FIA) EUDAMED
Model / Reference
5M13C2-25-EU, 5M13C2-50-EU EUDAMED

Identifiers

Primary DI / UDI-DI
D-5M13C2YU EUDAMED
Basic UDI-DI
B-5M13C2YU EUDAMED
EMDN Code
W0102160601 C-REACTIVE PROTEIN - RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

C-Reactive Protein Test (FIA) by Xiamen Boson Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000001096
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (2)

  • EUDAMED e175d41f-65bc-4028-88cb-5342b6bdecdf 61 fields · synced Jun 18, 2026
  • EUDAMED e175d41f-65bc-4028-88cb-5342b6bdecdf-1 61 fields · synced Jun 10, 2026