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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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Wall Lift — 4 UDI-DI variants, MDR (Handi-Move NV)

MD Atlas
Handi-Move NV

Data from EUDAMED, last updated May 23, 2026

Wall Lift

54040166WL7Z

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: Handi-Move NV

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 54040166WL7Z
Device name: Wall Lift
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Handi-Move NV
SRN: BE-MF-000016949
Country: Belgium
Email: info@handimove.com
Phone: +32 54 31 97 10

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JRW7C6470KG7J02T2W17J4T3

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

Wall Lift 6 cycle 110V05404016610454
Wall Lift 6 cycle 220V05404016610430
Wall Lift Heavy Duty 110V05404016610416
Wall Lift Heavy Duty 220V05404016610393