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Rubella And Measles Nucleic Acid Test Kit (Fluorescent Probe-based Real-time PC…

EUDAMED

Class IVD General (EU MDR)

Ref R07301T2048

by Jiangsu Mole Bioscience Co., LTD.

Identity

Device Name
Rubella And Measles Nucleic Acid Test Kit (Fluorescent Probe-based Real-time PCR Assay) EUDAMED
Model / Reference
R07301T2048 EUDAMED

Identifiers

Primary DI / UDI-DI
06970895475846 EUDAMED
Basic UDI-DI
B-06970895475846 EUDAMED
EMDN Code
W0105040104 RUBELLA - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Greece 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

Rubella And Measles Nucleic Acid Test Kit (Fluorescent Probe-based Real-time PC… by Jiangsu Mole Bioscience Co., LTD. — Class IVD General — IVDD — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000001539
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED d713417b-e3d3-4587-a9ac-50a7d6c10da6 61 fields · synced Jun 19, 2026