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Artron Treponema Pallidum (TP) Antibody Test

EUDAMED

Class C (EU MDR)

Ref A02-09-322PModel Cassette

by Artron Laboratories Inc.

Identity

Trade Name
Artron Treponema Pallidum (TP) Antibody Test EUDAMED
Device Name
Syphilis Test EUDAMED
Model / Reference
Cassette EUDAMED
A02-09-322P EUDAMED

Identifiers

Primary DI / UDI-DI
00628347561130 EUDAMED
Basic UDI-DI
62834756AL02090279 EUDAMED
EMDN Code
W0105090105 SYPHILIS - RT & POC EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Romania EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Artron Treponema Pallidum (TP) Antibody Test by Artron Laboratories Inc. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CA-MF-000028974
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 28513c10-ef51-44fa-9bd6-19315e535d97 61 fields · synced Jul 10, 2026