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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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HeliQ stationary lift — 6 UDI-DI variants, MDR (Human Care HC AB)

MD Atlas
Human Care HC AB

Data from EUDAMED, last updated May 30, 2026

HeliQ stationary lift

7331599LB55100H51150HXA

6 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: Human Care HC AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7331599LB55100H51150HXA
Device name: —
Device model: HeliQ stationary lift
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Human Care HC AB
SRN: SE-MF-000002090
Country: Sweden
Email: info.se@humancaregroup.com
Phone: +46 8 510 132 00

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KEYDC815JN65HG90NJX2NXKQ

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

HeliQ stationary lift 150kg EU07331599441107
HeliQ stationary lift 220kg Europe07331599441206
HeliQ stationary lift 300kg Europe07331599441305
HeliQ stationary lift PT (kit) 150kg Europe07331599441152
HeliQ stationary lift PT 220kg Europe07331599441251
HeliQ stationary lift PT 300kg Europe07331599441350