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Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Hybrid Capture-CLIA)

EUDAMED

Class C (EU MDR)

Ref DH3-096

by Hangzhou Dalton BioSciences, Ltd.

Identity

Trade Name
Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Hybrid Capture-CLIA) EUDAMED
Device Name
Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Hybrid Capture-CLIA) EUDAMED
Model / Reference
DH3-096 EUDAMED

Identifiers

Primary DI / UDI-DI
06973873140026 EUDAMED
Basic UDI-DI
697387314DH3SQ EUDAMED
Direct Marketing DI
06973873140026 EUDAMED
EMDN Code
W0105041003 PARTIAL GENOTYPING HIGH-RISK HPV - NA REAGENTS EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany 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

New Device

No

EUDAMED

Human Papillomavirus (HPV) Nucleic Acid Detection Kit (Hybrid Capture-CLIA) by Hangzhou Dalton BioSciences, Ltd. — Class C — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000036196
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 7501e8a0-8af9-4bb9-a269-eedd86e69e5e 61 fields · synced Jun 18, 2026