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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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Leichtlast — 7 UDI-DI variants, MDR (Ondal Medical Systems GmbH)

MD Atlas
Ondal Medical Systems GmbH

Data from EUDAMED, last updated May 23, 2026

Leichtlast

4061591000400QX

7 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: Ondal Medical Systems GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4061591000400QX
Device name: Leichtlast
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 2021

Manufacturer & authorised representative

Manufacturer

Name: Ondal Medical Systems GmbH
SRN: DE-MF-000000203
Country: Germany
Email: info@ondal.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01FK039Z2F5BH6T3W9RSMVHJS5

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

AC 200004061591000028
AC 7704061591000011
AC LCH04061591000035
AC Swing04061591000004
DB AC77/AC200004061591000073
DB Swing04061591000066
WB Swing, AC77, AC200004061591000042