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C-Peptide ELISA

EUDAMED

Class IVD General (EU MDR)

Ref CAN-C-P-4380Model 96 Tests

by Diagnostics Biochem Canada Inc.

Identity

Device Name
C-Peptide ELISA EUDAMED
Model / Reference
96 Tests EUDAMED
CAN-C-P-4380 EUDAMED

Identifiers

Primary DI / UDI-DI
++B261CANCP4380JH EUDAMED
Basic UDI-DI
B-++B261CANCP4380JH EUDAMED
EMDN Code
W0102060101 C-PEPTIDE 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

C-Peptide ELISA by Diagnostics Biochem Canada 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
CA-MF-000032449
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED f0868608-a5f6-4be9-8860-ead216bcb44f 61 fields · synced Jun 18, 2026