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RIDASCREEN® Calprotectin

EUDAMED

Class B (EU MDR)

Ref G09036Ref G09036C01-VK

by R-Biopharm AG

Identity

Device Name
RIDASCREEN® Calprotectin EUDAMED
Model / Reference
G09036 EUDAMED
G09036C01-VK EUDAMED

Identifiers

Primary DI / UDI-DI
04049095070051 EUDAMED
04049095070457 EUDAMED
Basic UDI-DI
4049095G090360000SL EUDAMED
EMDN Code
W0102019009 CALPROTECTIN EUDAMED

Classification

Device Class
Class B 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

New Device

No

EUDAMED

RIDASCREEN® Calprotectin by R-Biopharm AG — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
R-Biopharm AG
EUDAMED SRN
DE-MF-000007993

Sources (2)

  • EUDAMED 01a1091b-cb13-4340-8437-3851014ee19c 61 fields · synced Jul 11, 2026
  • EUDAMED 8ba4c23c-20d7-4dee-a949-0cc41bf18bca 61 fields · synced May 18, 2026