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Nucleic Acid Detection Kit for 16&18 Human Papillomavirus (HPV) Genotypes (PCR …

EUDAMED

Class IVD General (EU MDR)

Ref 106-0064-01Model 12 reactions/kit

by Igenesis(Shanghai)Co., Ltd.

Identity

Device Name
Nucleic Acid Detection Kit for 16&18 Human Papillomavirus (HPV) Genotypes (PCR fluorescence probe method) EUDAMED
Model / Reference
12 reactions/kit EUDAMED
106-0064-01 EUDAMED

Identifiers

Primary DI / UDI-DI
06975447582140 EUDAMED
Basic UDI-DI
B-06975447582140 EUDAMED
EMDN Code
W0105041002 SCREENING HIGH-RISK HPV - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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 16&18 Human Papillomavirus (HPV) Genotypes (PCR … by Igenesis(Shanghai)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-000001552
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 1030ad2d-6a7f-4263-933f-b76f3661b031 61 fields · synced Jun 18, 2026