← Back to catalogue

C-Reactive Protein Kit (Immunoturbidimetric Method)

EUDAMED

Class C (EU MDR)

Ref 3011001

by Zybio Inc.

Identity

Device Name
C-Reactive Protein Kit (Immunoturbidimetric Method) EUDAMED
Model / Reference
3011001 EUDAMED

Identifiers

Primary DI / UDI-DI
06941967227038 EUDAMED
Basic UDI-DI
69732628630110*********XH EUDAMED
EMDN Code
W01021109 C-REACTIVE PROTEIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

New Device

No

EUDAMED

C-Reactive Protein Kit (Immunoturbidimetric Method) by Zybio Inc. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Zybio Inc.
EUDAMED SRN
CN-MF-000003349
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 3c70ec53-b350-4d95-a72b-83a7f12d4d0e 61 fields · synced Jun 18, 2026