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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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Light Incontinence Devices — 267 UDI-DI variants, MDR (Ontex BV)

MD Atlas
Ontex BV

Data from EUDAMED, last updated May 23, 2026

Light Incontinence Devices

5414874LightIncoH6

267 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: Ontex BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5414874LightIncoH6
Device name: Light Incontinence Devices
Device model: Light Inco
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: Ontex BV
SRN: BE-MF-000003544
Country: Belgium
Email: chloe.vandevelde@ontexglobal.com
Phone: +32 476 06 29 44

Variants by status

UDI-DI variants

267 UDI-DI variants

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Applied filters

basicUdiUlid01HWQ39RSWVR1WDY0NHS31YMTV

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

No registered UDI-DI variants for this device family.