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MosaiQ® AiPlex CTD

EUDAMED

Class B (EU MDR)

Ref 160002

by AliveDx Suisse SA

Identity

Trade Name
MosaiQ® AiPlex CTD EUDAMED
Device Name
MosaiQ® AiPlex CTD EUDAMED
Model / Reference
160002 EUDAMED

Identifiers

Primary DI / UDI-DI
07640327462032 EUDAMED
Basic UDI-DI
764032746CTDPLEX13M EUDAMED
EMDN Code
W0102100199 AUTOIMMUNE CONNECTIVE TISSUE DISEASES TESTING - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

New Device

No

EUDAMED

MosaiQ® AiPlex CTD by AliveDx Suisse SA — Class B — 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

Manufacturer
AliveDx Suisse SA
EUDAMED SRN
CH-MF-000024025
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 0fde658a-5170-4151-b6fc-55364362239a 61 fields · synced Jun 19, 2026