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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

v1.0.0 — Class IIa MDR by AUGMENTED REALITY…

MD Atlas
AUGMENTED REALITY SOFTWARE SL

EUDAMED last updated this device on May 14, 2026

v1.0.0

8437027533LAIAXRAS

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AUGMENTED REALITY SOFTWARE SL
UDI-DI code: 08437027533006
Reference / catalog number: v1.0.0

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Manufacturer information

Organization name: AUGMENTED REALITY SOFTWARE SL
SRN: ES-MF-000044174
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 14, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437027533006
Basic UDI-DI: 8437027533LAIAXRAS
Reference / catalog number: v1.0.0
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: LAIA XR is a medical imaging analysis software intended for the processing, review, analysis, and manipulation of patient-specific 3D reconstructions, generated from medical imaging data, to assist surgeons of any medical specialty in surgical planning, by enhancing the understanding and evaluation of each patient anatomy, through both, desktop and Virtual Reality (VR) environments.
Additional information URL: https://laiaxr.com/soporte/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

This device is not currently linked to any other device.

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.