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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

EyableEye — Class I MDR by ASARIA

MD Atlas
ASARIA

EUDAMED last updated this device on Sep 23, 2025

EyableEye

3770039113V1.0T7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ASARIA
UDI-DI code: 03770039113008
Reference / catalog number: V1.0

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Manufacturer information

Organization name: ASARIA
SRN: FR-MF-000047945
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: EyableEye
UDI-DI code: 03770039113008
Basic UDI-DI: 3770039113V1.0T7
Reference / catalog number: V1.0
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: Application PC de traitement des flux entrant et sortant et de traitement des données d’intervention chirurgicale, cartes d’acquisitions des flux vidéo des autres moniteurs et routeur wifi de connexion complètent ce système. L’application communique avec un casque de réalité augmentée.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039004TELEVISION SYSTEMS

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.