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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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Mobile lift, battery-powered — 5 UDI-DI variants, MDR

MD Atlas
Liko Aktiebolag

Data from EUDAMED, last updated May 31, 2026

Mobile lift, battery-powered

0887761GMN000034U5

5 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: Liko Aktiebolag

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0887761GMN000034U5
Device name: Mobile lift, battery-powered
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Liko Aktiebolag
SRN: SE-MF-000001404
Country: Sweden
Email: quality_lulea@baxter.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KCQ3J40ZDVHB457NR9XSSAZS

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

Golvo00887761981737
Golvo00887761981751
Viking00887761981867
Viking00887761981874
Viking00887761981850