Is Psylaris certified as a medical device?
Psylaris by EMDR-VR B.V. is listed in EUDAMED as a CE class IIa medical device. No notified body certificate is visible in EUDAMED yet; ask the maker for it (devices still under the older MDD rules often have none listed). We found no FDA authorisation.
At a glance
| Product | Psylaris |
|---|---|
| Maker | EMDR-VR B.V. |
| Care area | Mental health |
| What it does | Virtual reality EMDR therapy for trauma, used together with a therapist |
| FDA | No FDA authorisation found |
| EU (CE) | Class IIa |
| EU certificate | Not visible in EUDAMED yet (checked 18 October 2026) |
| Website | psylaris.com |
| Status | CE verified |
| Last checked | 7 October 2026 |
Need the evidence behind this entry?
Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes
Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes
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