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MMP-3 Rapid Test (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref P232101

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
MMP-3 Rapid Test (FIA) EUDAMED
Device Name
MMP-3 Rapid Test (FIA) EUDAMED
Model / Reference
P232101 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698600781 EUDAMED
Basic UDI-DI
B-16972698600781 EUDAMED
EMDN Code
W0102039010 MATRIX-METALLOPROTEINASES EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain 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

MMP-3 Rapid Test (FIA) by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd. — 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
CN-MF-000013495
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED f11d8d6f-81d6-4dc2-8604-71bbc1897966 61 fields · synced Jun 18, 2026