Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

MosaiQ® AiPlex CTDplus — 3 UDI-DI variants, IVDR (AliveDx Suisse SA)

MD Atlas
AliveDx Suisse SA

Data from EUDAMED, last updated May 23, 2026

MosaiQ® AiPlex CTDplus

764032746CTDPLUSMAGH5

3 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Clinical investigations

Investigation number: 2024022001343900
Registered: No
Countries: United Kingdom

Identity & classification

Basic UDI-DI: 764032746CTDPLUSMAGH5
Device name: MosaiQ® AiPlex CTDplus
Device model: 1x250, 4x85, 1x85
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Feb 11, 2026

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

3 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01JMCTBMSRG16RNDMXV3VS4BPF

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

MosaiQ® AiPlex CTDplus07640327462070
16000907640327462308
MosaiQ® AiPlex CTDplus07640327462087