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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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Liftolet — 4 UDI-DI variants, MDR (ATO FORM GmbH)

MD Atlas
ATO FORM GmbH

Data from EUDAMED, last updated May 23, 2026

Liftolet

42511106LIFTOLETMN

4 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: ATO FORM GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42511106LIFTOLETMN
Device name: Liftolet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: ATO FORM GmbH
SRN: DE-MF-000008880
Country: Germany
Email: r.friedrich@ato-form.com
Phone: +49 6093 944-266

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KS2501HW20V2E6GSKHR66AZ9

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

LT-100004251110627854
LT-1000-TD04251110627885
LT-1000-S04251110627861
LT-1000-T04251110627878