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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 Multi-Discipline Automated… — 3 UDI-DI variants, IVDR

MD Atlas
ImmunoDiagnostic Systems France

Data from EUDAMED, last updated May 19, 2026

IDS-iSYS Multi-Discipline Automated System

3760173851003YL

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 France

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 3760173851003YL
Device name: IDS-iSYS Multi-Discipline Automated System
Device model: IS-310400
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: ImmunoDiagnostic Systems France
SRN: FR-MF-000023843
Country: France
Email: anne.vaillant@revvity.com
Phone: +33380905252

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G38QZAY6EX28G4XS31SKCXWF

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

IS-31040003760173851003
TGS0000103760173851058
4267503760173851034