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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

REAtouch Lite 2 — Class I MDR by Axinesis

MD Atlas
Axinesis

EUDAMED last updated this device on Mar 4, 2026

REAtouch Lite 2

5430003042REAtouchLite2R7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Axinesis
UDI-DI code: 05430003042045
Reference / catalog number: REAtouch Lite 2

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Manufacturer information

Organization name: Axinesis
SRN: BE-MF-000018870
Manufacturer status: Active

Related devices

REAplanB-05430003042007On the market REAtouch5430003042REAtouch4LOn the market REAtouch Lite5430003042REAtouch4LOn the market REAtouch Oboc5430003042REAtouchObocX3On the market touchLAB5430003042touchLABAVOn 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 3 countries total.

Country	On market since	Until
BelgiumPrimary placement		Still on market
France		Still on market
Netherlands		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05430003042045
Basic UDI-DI: 5430003042REAtouchLite2R7
Reference / catalog number: REAtouch Lite 2
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
Y0504ARMS, TORSO AND LEGS RE-EDUCATION DEVICES

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
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Software identification