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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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Veya Dx — 2 UDI-DI variants, IVDR (Tecan Schweiz AG)

MD Atlas
Tecan Schweiz AG

Data from EUDAMED, last updated May 23, 2026

Veya Dx

764013748IVS10080000AEC

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Tecan Schweiz AG

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 764013748IVS10080000AEC
Device name: —
Device model: Veya Dx
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Tecan Schweiz AG
SRN: CH-MF-000044877
Country: Switzerland
Email: RA-Instrumentation@tecan.com
Phone: +41 44 922 81 11

Authorised representative

Name: Tecan Austria GmbH
SRN: AT-AR-000044488
Country: Austria
Phone: +43 6246 8933 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JYDZQWYNRZQNS0XHSNPG61BH

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

Veya Dx 607640137480288
Veya Dx 907640137480295