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INNODX ProGRP CMIA

EUDAMED

Class C (EU MDR)

Ref KR-ProGRP-0450

by Xiamen Innodx Biotech Co., Ltd.

Identity

Trade Name
INNODX ProGRP CMIA EUDAMED
Device Name
INNODX ProGRP CMIA EUDAMED
Model / Reference
KR-ProGRP-0450 EUDAMED

Identifiers

Primary DI / UDI-DI
06973600799763 EUDAMED
Basic UDI-DI
697360079024JV EUDAMED
EMDN Code
W0102030121 PRO-GASTRIN-RELEASING PEPTIDE EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

INNODX ProGRP CMIA by Xiamen Innodx Biotech Co., Ltd. — Class C — 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

EUDAMED SRN
CN-MF-000041071
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 09636bc8-c90b-4a44-a2a6-2c3e9bb058fc 61 fields · synced Jun 18, 2026