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Ureaplasma urealyticum (UU) and Neisseria Gonorrhoeae (NG) Diagnostic Kit (PCR-…

EUDAMED

Class IVD General (EU MDR)

Ref 18-01-0007Model 48 Tests/kit

by Shenzhen Zijian Biotechnology Co., Ltd

Identity

Trade Name
Ureaplasma urealyticum (UU) and Neisseria Gonorrhoeae (NG) Diagnostic Kit (PCR-Fluorescence Probing) EUDAMED
Device Name
Ureaplasma urealyticum (UU) and Neisseria Gonorrhoeae (NG) Diagnostic Kit (PCR-Fluorescence Probing) EUDAMED
Model / Reference
48 Tests/kit EUDAMED
18-01-0007 EUDAMED

Identifiers

Primary DI / UDI-DI
06974674892473 EUDAMED
Basic UDI-DI
B-06974674892473 EUDAMED
EMDN Code
W0105070201 GRAM+ - GRAM- - FUNGI - MULTIPLEX 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

Ureaplasma urealyticum (UU) and Neisseria Gonorrhoeae (NG) Diagnostic Kit (PCR-… by Shenzhen Zijian Biotechnology Co., Ltd — Class IVD General — IVDD — listed…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000022829
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 53da2c23-f818-4284-9809-763894d6babb 61 fields · synced Oct 6, 2026