Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Wall Lift Heavy Duty 220V — Class I MDR by Handi-Move NV

MD Atlas
Handi-Move NV

EUDAMED last updated this device on Apr 15, 2025

Wall Lift Heavy Duty 220V

54040166WL7Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Handi-Move NV
UDI-DI code: 05404016610393
Reference / catalog number: 2420 00000001

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Handi-Move NV
SRN: BE-MF-000016949
Manufacturer status: Active

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement	Sep 1, 2020	Still on market

Device identification

Trade name: Wall Lift Heavy Duty 220V
UDI-DI code: 05404016610393
Basic UDI-DI: 54040166WL7Z
Reference / catalog number: 2420 00000001
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Wall Lift 2420
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050302ELECTRIC FIXED LIFTS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

Active Sling Extra Large for 262054040166NRBSK5On the market Active Sling Extra Large for 2620 customized54040166NRBSK5On the market Active Sling Extra Small for 262054040166NRBSK5On the market Active Sling Extra Small for 2620 customized54040166NRBSK5On the market Active Sling Large for 162054040166MBLSHCOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.