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Fully Automated PCR Detection System

EUDAMED

Class A (EU MDR)

Ref AutoPoc MDx

by Zhuhai Shineway Biotech Co., Ltd

Identity

Device Name
Fully Automated PCR Detection System EUDAMED
Model / Reference
AutoPoc MDx EUDAMED

Identifiers

Primary DI / UDI-DI
16974900600169 EUDAMED
Basic UDI-DI
697490060AutoPocMDx2S EUDAMED
Direct Marketing DI
16974900600169 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy 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

Category: Nucleic acid sample preparation instrument IVD

Fully Automated PCR Detection System by Zhuhai Shineway Biotech Co., Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000027278
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 346499be-4bbf-4650-8591-0975207eb6fa 61 fields · synced Jun 17, 2026