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Exdia CRP

EUDAMED

Class IVD General (EU MDR)

Ref PR-FC06

by Precision Biosensor Inc.

Identity

Device Name
Exdia CRP EUDAMED
Model / Reference
PR-FC06 EUDAMED

Identifiers

Primary DI / UDI-DI
08800026300151 EUDAMED
Basic UDI-DI
B-08800026300151 EUDAMED
EMDN Code
W01021109 C-REACTIVE PROTEIN 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

Yes

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Exdia CRP by Precision Biosensor Inc. — 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
KR-MF-000034861
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED 6c54a2f6-fcc6-4fcd-a55e-8ebf903e56d6 61 fields · synced Jul 14, 2026