gudid Primary ID: N-140 (Rotate)

VRPhysio (UDI N-140 (Rotate))

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VRPhysio (Model/Catalog Number: N-140 (Rotate)) 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: N-140 (Rotate)
Product Code / EMDN: ISD
Device Name: A software-only medical device intended for cervical region rehabilitation. The software tracks motion and movement kinematics and guides patients in the performance of physical exercises according to their treating medical practitioner's guidelines. The N-140 is a prescription-only device that can be used in clinical setting or at home, with or without the assistance of clinician. N-140 does not provide a report that analyzes the measurements, makes medical diagnoses, or recommends treatment.
Database Sync Date: 2026-08-09 09:18:17

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of VRPhysio?

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

What is the Primary UDI-DI identifier for VRPhysio?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N-140 (Rotate).

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

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