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VRPhysio

FDA UDI

Class II (US FDA UDI)

by Xr Health Il Ltd

Identity

Trade Name
VRPhysio FDA UDI
Generic Name
Biomechanical function analysis/rehabilitation software FDA UDI
Device Name
A software-only medical device intended for upper extremity and full body conventional rehabilitation. The software tracks motion and movement kinematics and guides patients in the performance of motor-cognitive exercises according to their treating medical practitioner's guidelines. FDA UDI
Model / Reference
MC-310 (Color Match) FDA UDI
Description
A software-only medical device intended for upper extremity and full body conventional rehabilitation. The software tracks motion and movement kinematics and guides patients in the performance of motor-cognitive exercises according to their treating medical practitioner's guidelines. FDA UDI

Identifiers

Primary DI / UDI-DI
07290016986044 FDA UDI
FDA Product Code
ISD FDA UDI
GMDN Term
Biomechanical function analysis/rehabilitation software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5360 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

VRPhysio by Xr Health Il Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xr Health Il Ltd

Sources (1)

  • FDA UDI 351046e1-108c-4d97-90d9-039e301c6c00 35 fields · synced May 30, 2026