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Organization name
UDI-DI code
Reference / catalog number

Active Sling Medium for 2620… — Class I MDR by Handi-Move NV

MD Atlas
Handi-Move NV

EUDAMED last updated this device on Apr 28, 2025

Active Sling Medium for 2620 customized

54040166NRBSK5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Handi-Move NV
UDI-DI code: 05404016612755
Reference / catalog number: 3406M 90000001

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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: Active Sling Medium for 2620 customized
UDI-DI code: 05404016612755
Basic UDI-DI: 54040166NRBSK5
Reference / catalog number: 3406M 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: Active Sling 3406 M customized
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

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