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HypnoVR System

by Ybia SAS 19 variants

Ref HVR-G3-M9-E500-R

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3770022767HypnoVRSNG Basic UDI-DI 03770022767379UDI-DIDate11 Oct 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
HVR-G3-M9-E500-R
Primary DI / UDI-DI
03770022767379
Basic UDI-DI
3770022767HypnoVRSNG
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Medical Purpose
HypnoVR is a virtual reality hypnosis solution intended to improve management of patients’ pain, stress and anxiety by providing an alternative or complementary solution to chemical treatments. HypnoVR is used with a virtual reality headset, an audio headset, and a tablet.

Manufacturer details

EUDAMED SRN
FR-PR-000029204

Other devices from Ybia SAS

See all devices from Ybia SAS →

Properties

Other properties (1)

  • Sterile: No