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

Sling; children ; version… — Class I MDR by Handi-Move NV

MD Atlas
Handi-Move NV

EUDAMED last updated this device on Apr 28, 2025

Sling; children ; version butterfly ; M ; patient matched

54040166NRBSK5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Handi-Move NV
UDI-DI code: 05404016613776
Reference / catalog number: 3552M 90000001

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

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.

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement	May 12, 2021	Still on market

Device identification

Trade name: Sling; children ; version butterfly ; M ; patient matched
UDI-DI code: 05404016613776
Basic UDI-DI: 54040166NRBSK5
Reference / catalog number: 3552M 90000001
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: Sling 3552 M ; patient matched
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0805038002NON-RIGID SUPPORTS FOR LIFTS (HARNESSES)

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