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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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Organization name
UDI-DI code
Reference / catalog number

Footscan Pro Small — Class I MDR by Materialise Motion

MD Atlas
Materialise Motion

EUDAMED last updated this device on Jan 14, 2026

Footscan Pro Small

542502600B001UN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Materialise Motion
UDI-DI code: 05425026002008
Reference / catalog number: Footscan Pro Small

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Manufacturer information

Organization name: Materialise Motion
SRN: BE-MF-000026574
Manufacturer status: Active

Related devices

Footscan Pro Medium542502600B001UNOn the market Footscan Pro Medium Sync542502600B001UNOn the market Footscan Pro Small Sync542502600B001UNOn the market v26.1542502600B002UQOn 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.

Placed on the market in Belgium; per-country availability dates not published.

Device identification

Trade name: Footscan Pro Small
UDI-DI code: 05425026002008
Basic UDI-DI: 542502600B001UN
Reference / catalog number: Footscan Pro Small
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12062603SENSOR-BASED PLATFORMS

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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Manufacturing date
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Software identification