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Treponema Pallidum Antibody Detection Kit (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref 3010664Model 1×50 Tests/kit

by Dirui Industrial Co., Ltd

Identity

Trade Name
Treponema Pallidum Antibody Detection Kit (Chemiluminescence Immunoassay) EUDAMED
Device Name
Treponema Pallidum Antibody Detection Kit (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
1×50 Tests/kit EUDAMED
3010664 EUDAMED

Identifiers

Primary DI / UDI-DI
06925794518873 EUDAMED
Basic UDI-DI
B-06925794518873 EUDAMED
EMDN Code
W0105010302 SYPHILIS ANTIBODY ASSAYS TOTAL EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

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

Treponema Pallidum Antibody Detection Kit (Chemiluminescence Immunoassay) by Dirui Industrial 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-000001891
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED dde513a2-4853-4871-8a42-eeed22bf8cc3 61 fields · synced Jun 17, 2026