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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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IWT — 2 UDI-DI variants, MDR (Barco NV)

MD Atlas
Barco NV

Data from EUDAMED, last updated May 23, 2026

IWT

5415334_IWT_55

2 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5415334_IWT_55
Device name: IWT
Device model: Intuitive workflow tools SW
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Oct 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: Barco NV
SRN: BE-MF-000000690
Country: Belgium
Email: eric.caus@barco.com
Phone: +3256233349

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JB9JVQXVYAXKN5MH06GYDF9E

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

Barco05415334058415
Barco05415334002050