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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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LiftKar PT — 2 UDI-DI variants, MDR (Sano Transportgeraete GmbH)

MD Atlas
Sano Transportgeraete GmbH

Data from EUDAMED, last updated May 23, 2026

LiftKar PT

912004777PTS2

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: Sano Transportgeraete GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 912004777PTS2
Device name: LiftKar PT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sano Transportgeraete GmbH
SRN: AT-MF-000053609
Country: Austria
Email: office@sano.at

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQVQYCK1JRRPJE1Q9BG24HCT

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

04572109120047770214
04572209120047770221