← Back to catalogue

Treponema Pallidum Antibody(Anti-TP)Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref 69543760F000636HModel 100 Tests

by Beijing Leadman Biochemistry Co., Ltd.

Identity

Trade Name
Treponema Pallidum Antibody(Anti-TP)Assay Kit EUDAMED
Device Name
Treponema Pallidum Antibody(Anti-TP)Assay Kit EUDAMED
Model / Reference
100 Tests EUDAMED
69543760F000636H EUDAMED

Identifiers

Primary DI / UDI-DI
06954376005463 EUDAMED
Basic UDI-DI
B-06954376005463 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

Yes

EUDAMED

Microbial Substances

Yes

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)Assay Kit by Beijing Leadman Biochemistry Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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-000020150
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 1e85c5a3-b3fe-477d-8b12-5e823084623b 61 fields · synced Jun 19, 2026