← Back to catalogue

Treponema Pallidum Antibody (Anti-TP) Detection Kit(Magnetic Solid Phase Chemil…

EUDAMED

Class IVD General (EU MDR)

Ref 50 Tests/kit(DR1140-1)Model 50 Tests/kit

by Biobase Diagnostic Technology (Shandong) Co., Ltd.

Identity

Trade Name
Treponema Pallidum Antibody (Anti-TP) Detection Kit(Magnetic Solid Phase ChemiluminescentImmunoassay) EUDAMED
Device Name
Treponema Pallidum Antibody (Anti-TP) Detection Kit(Magnetic Solid Phase ChemiluminescentImmunoassay) EUDAMED
Model / Reference
50 Tests/kit EUDAMED
50 Tests/kit(DR1140-1) EUDAMED

Identifiers

Primary DI / UDI-DI
06974969982919 EUDAMED
Basic UDI-DI
B-06974969982919 EUDAMED
EMDN Code
W0105010302 SYPHILIS ANTIBODY ASSAYS TOTAL 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

Treponema Pallidum Antibody (Anti-TP) Detection Kit(Magnetic Solid Phase Chemil… by Biobase Diagnostic Technology (Shandong) Co., Ltd. — Class IVD General…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000025964
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 99079355-9b54-4ffa-82af-e5b1e0cfece8 61 fields · synced Oct 6, 2026