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PCR-based Ureaplasma Urealyticum Test Kit (Fluorometric PCR)

EUDAMED

Class IVD General (EU MDR)

Ref ID024

by Beijing Applied Biological Technologies Co., Ltd.

Identity

Device Name
PCR-based Ureaplasma Urealyticum Test Kit (Fluorometric PCR) EUDAMED
Model / Reference
ID024 EUDAMED

Identifiers

Primary DI / UDI-DI
06974323012986 EUDAMED
Basic UDI-DI
B-06974323012986 EUDAMED
EMDN Code
W010501080303 UREAPLASMA DETECTION BY 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

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

PCR-based Ureaplasma Urealyticum Test Kit (Fluorometric PCR) by Beijing Applied Biological Technologies 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-000012338
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 74a94df8-0280-436d-b768-6ea86617e62c 61 fields · synced Jul 25, 2026