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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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IDS-iSYS System Liquid (Syst.l) — 3 UDI-DI variants, IVDR

MD Atlas
Immunodiagnostic Systems SA

Data from EUDAMED, last updated May 23, 2026

IDS-iSYS System Liquid (Syst.l)

5425030421017RC

3 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: Immunodiagnostic Systems SA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 5425030421017RC
Device name: IDS-iSYS System Liquid (Syst.l)
Device model: IS-CS100
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: Immunodiagnostic Systems SA
SRN: BE-MF-000015341
Country: Belgium
Email: info.be@idsplc.com
Phone: +3242522636

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G56SVWD4CTG452D3AKCN1XMW

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

i-Track 10 System Liquid05425030420010
IDS-iSYS System Liquid (Syst. l)05425030421017
System Liquid 5L05425030420065