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Nucleic Acid Detection Kit for High-risk Human Papillomavirus (Typing) (PCR-Flu…

EUDAMED

Class IVD General (EU MDR)

Ref HPV002-48

by Singuway Biotech Inc.

Identity

Trade Name
Nucleic Acid Detection Kit for High-risk Human Papillomavirus (Typing) (PCR-Fluorescence Probing) EUDAMED
Device Name
Nucleic Acid Detection Kit for High-risk Human Papillomavirus (Typing) (PCR-Fluorescence Probing) EUDAMED
Model / Reference
HPV002-48 EUDAMED

Identifiers

Primary DI / UDI-DI
06974081870378 EUDAMED
Basic UDI-DI
B-06974081870378 EUDAMED
EMDN Code
W0105041002 SCREENING HIGH-RISK HPV - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Nucleic Acid Detection Kit for High-risk Human Papillomavirus (Typing) (PCR-Flu… by Singuway Biotech Inc. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000027180
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED a1fba60c-1435-41b3-955c-ad7a1d529173 61 fields · synced Jun 17, 2026