gudid
Primary ID: MT-220 (Balloon Blast)
VRPhysio (UDI MT-220 (Balloon Blast))
Manufactured by XR HEALTH IL LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VRPhysio - Primary ID MT-220 (Balloon Blast)
Device Regulatory Overview
The VRPhysio (Model/Catalog Number: MT-220 (Balloon Blast)) 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
- MT-220 (Balloon Blast)
- Product Code / EMDN
- ISD
- Device Name
- A software-only medical device intended for upper extremity and full body 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 MT-220 is a prescription-only device that can be used in clinical setting or at home, with or without the assistance of clinician. MT-220 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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Get API Token Access ($49/mo)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 MT-220 (Balloon Blast).
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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