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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

Healthy Mind VR — Class I MDR by Healthy Mind

MD Atlas
Healthy Mind

EUDAMED last updated this device on Dec 15, 2025

Healthy Mind VR

3770022927HealthyMindVR59

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Healthy Mind
UDI-DI code: 03770022927025
Reference / catalog number: HMVR Portable

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Manufacturer information

Organization name: Healthy Mind
SRN: FR-MF-000012757
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW011
The use of the headset by pregnant women, patients with vision disorders, epilepsy (or epileptic symptoms), migraines, psychiatric disorders such as schizophrenia, schizophreniform disorders or major neurocognitive disorders such as dementia, incompatible neurological disorders, as well as persons wearing a pacemaker is subject to the advice of a physician.
CW010
EUDAMED did not publish a description for this code.

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: Healthy Mind VR
UDI-DI code: 03770022927025
Basic UDI-DI: 3770022927HealthyMindVR59
Reference / catalog number: HMVR Portable
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: https://drive.google.com/drive/folders/1EcW06xr8FCuH58zGDRQukY4NEtx-KPEt?usp=drive_link
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.