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Galaxy Pro

EUDAMED

Class A (EU MDR)

Ref 101-0037-01Model Galaxy

by Igenesis(Shanghai)Co., Ltd.

Identity

Trade Name
Galaxy Pro EUDAMED
Device Name
Automated Fully Enclosed qPCR Instrument EUDAMED
Model / Reference
Galaxy EUDAMED
101-0037-01 EUDAMED

Identifiers

Primary DI / UDI-DI
06975447581037 EUDAMED
Basic UDI-DI
697544758GALAXYU9 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Greece EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Galaxy Pro by Igenesis(Shanghai)Co., Ltd. — Class A — 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-000001552
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED b9632ba7-aea9-4c6e-9129-a8d123443ddd 61 fields · synced Jun 19, 2026