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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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Silicon Touch — 2 UDI-DI variants, MDR (Naqi NV)

MD Atlas
Naqi NV

Data from EUDAMED, last updated May 23, 2026

Silicon Touch

542502989STUJ

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Naqi NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 542502989STUJ
Device name: Silicon Touch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: Naqi NV
SRN: BE-MF-000001241
Country: Belgium
Email: info@naqi.com
Phone: +32(0)13460190

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GPRAN01YWMN7GA2YHTPFAZ74

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

ST1505425029890145
Silicon Touch shipper15425029890142