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MosaiQ® AiPlex CD

EUDAMED

Class B (EU MDR)

Ref 160010Model 1x250, 4x85

by AliveDx Suisse SA

Identity

Trade Name
MosaiQ® AiPlex CD EUDAMED
Device Name
MosaiQ® AiPlex CD EUDAMED
Model / Reference
1x250, 4x85 EUDAMED
160010 EUDAMED

Identifiers

Primary DI / UDI-DI
07640327462049 EUDAMED
Basic UDI-DI
764032746AIPLEXCDMAGXK EUDAMED
Direct Marketing DI
07640327462049 EUDAMED
EMDN Code
W0102100699 CELIAC DISEASE - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Netherlands 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

New Device

No

EUDAMED

MosaiQ® AiPlex CD 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 995d79f6-6e61-455d-9b89-db1fbee4fe8f 61 fields · synced Jul 18, 2026