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Human papillomavirus (HPV) Nucleic Acid Detection kit

EUDAMED

Class IVD General (EU MDR)

Ref 32tests/kit

by CapitalBio Technology (Chengdu) Co., Ltd.

Identity

Device Name
Human papillomavirus (HPV) Nucleic Acid Detection kit EUDAMED
Model / Reference
32tests/kit EUDAMED

Identifiers

Primary DI / UDI-DI
06972221450886 EUDAMED
Basic UDI-DI
B-06972221450886 EUDAMED
EMDN Code
W0105041004 FULL GENOTYPING HIGH-RISK + LOW-RISK HPV - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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

Human papillomavirus (HPV) Nucleic Acid Detection kit by CapitalBio Technology (Chengdu) Co., Ltd. — 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-000027694
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 4ad23163-b5bf-4102-8dd3-576c09906bfc 61 fields · synced Jun 18, 2026