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Rapid Human Papillomavirus (16/18/45) DNA Test

EUDAMED

Class IVD General (EU MDR)

Ref RHPV301-AHG5E/RHPV301-AHG25E

by Healgen Scientific Limited Liability Company

Identity

Device Name
Rapid Human Papillomavirus (16/18/45) DNA Test EUDAMED
Model / Reference
RHPV301-AHG5E/RHPV301-AHG25E EUDAMED

Identifiers

Primary DI / UDI-DI
D-81649002RHPV301RBBS EUDAMED
Basic UDI-DI
B-81649002RHPV301RBBS EUDAMED
EMDN Code
W0105041005 OTHER HPV - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Rapid Human Papillomavirus (16/18/45) DNA Test by Healgen Scientific Limited Liability Company — 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
US-MF-000018839
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 262de5c9-4320-44f6-bc60-2e7c6769bd9d 61 fields · synced Oct 6, 2026