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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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MosaiQ® AiPlex VAS — 2 UDI-DI variants, IVDR (AliveDx Suisse SA)

MD Atlas
AliveDx Suisse SA

Data from EUDAMED, last updated May 23, 2026

MosaiQ® AiPlex VAS

764032746AIPLEXVASMAG7P

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: AliveDx Suisse SA

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Device characteristics

ReagentProfessional testing

Clinical investigations

Investigation number: AiPlex VAS-CPSP-1057B, Aiplex_VAS-CPSP-1059, Aiplex_VAS-CPSP-1060
Registered: No
Countries: United Kingdom

Registered: No

Identity & classification

Basic UDI-DI: 764032746AIPLEXVASMAG7P
Device name: MosaiQ® AiPlex VAS
Device model: 1x250, 4x85
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Aug 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: AliveDx Suisse SA
SRN: CH-MF-000024025
Country: Switzerland
Email: MosaiQ.RA-ch@alivedx.com

Authorised representative

Name: Emergo Europe B.V.
SRN: NL-AR-000000116
Country: Netherlands
Phone: +31 70 345 8570

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K1T08R7N6VKQT9GTXSTKERYX

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

16004007640327462186
16004107640327462209