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Ureaplasma Urealyticum (UU) Nucleic Acid Detection Kit (Fluorescent PCR Method)

EUDAMED

Class IVD General (EU MDR)

Ref 48 tests/kit

by CapitalBio Technology (Chengdu) Co., Ltd.

Identity

Device Name
Ureaplasma Urealyticum (UU) Nucleic Acid Detection Kit (Fluorescent PCR Method) EUDAMED
Model / Reference
48 tests/kit EUDAMED

Identifiers

Primary DI / UDI-DI
06972221451173 EUDAMED
Basic UDI-DI
B-06972221451173 EUDAMED
EMDN Code
W0105011699 BACTERIOLOGY - NA REAGENTS - OTHER 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

Ureaplasma Urealyticum (UU) Nucleic Acid Detection Kit (Fluorescent PCR Method) by CapitalBio Technology (Chengdu) Co., Ltd. — Class IVD General — IVDD…

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 ed3ce0ab-940f-4cdc-9b3e-69a489e6a909 61 fields · synced Jun 18, 2026