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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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Bodenplatte geschlossen für Liftolet — 8 UDI-DI variants, MDR

MD Atlas
ATO FORM GmbH

Data from EUDAMED, last updated May 23, 2026

Bodenplatte geschlossen für Liftolet

42511106LIFTOLETZUBJS

8 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: 42511106LIFTOLETZUBJS
Device name: Bodenplatte geschlossen für 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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS25016W6T9HPBY6V5A5GCEF

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-010004251110627762
LT-0100-104251110627779
LT-0100-S04251110627793
LT-0100-1S04251110627786
LT-012004251110627809
LT-0150-104251110627823
LT-015004251110627816
LT-020004251110627847