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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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LAight-Kontaktgel 5l Beutel — 2 UDI-DI variants, MDR (LENICURA GmbH)

MD Atlas
LENICURA GmbH

Data from EUDAMED, last updated May 23, 2026

LAight-Kontaktgel 5l Beutel

426237507EP001-01VL

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: LENICURA GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426237507EP001-01VL
Device name: LAight-Kontaktgel 5l Beutel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: LENICURA GmbH
SRN: DE-MF-000021196
Country: Germany
Email: service@lenicura.de
Phone: +49 611 95008500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G36JD4SPARJMM54AW4WD22D4

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

VK10006904262375070699
VK10006504262375070651