gudid Primary ID: VRET-910 (Expose)

VRBehavior (UDI VRET-910 (Expose))

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The VRBehavior (Model/Catalog Number: VRET-910 (Expose)) is a medical device manufactured by XR HEALTH IL LTD. This product is indexed under FDA Product Code / Category Classification ISD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VRET-910 (Expose)
Product Code / EMDN: ISD
Device Name: The VRET-910 "Expose" is a prescription-only medical software used as a tool by Licensed Healthcare Provider (LHP) in order to immerse their patients into virtual reality (VR) and 360 degree simulated environments, as part of remote or in-person therapy sessions devised to improve certain mental health conditions. The software can be used in clinical settings or at home, with or without the assistance of a licensed healthcare provider.
Database Sync Date: 2026-08-09 09:18:17

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of VRBehavior?

The registered manufacturer of record for VRBehavior is XR HEALTH IL LTD.

What is the Primary UDI-DI identifier for VRBehavior?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VRET-910 (Expose).

What classification code is assigned to this device?

This device is registered under product classification code ISD.

Similar Classification Devices (ISD)

Other Devices by XR HEALTH IL LTD

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint