w_CTSIB

GUDID 03760310780302

VIRTUALIS

Biomechanical function analysis/rehabilitation software

• Primary Device ID: 03760310780302
• NIH Device Record Key: efa117a8-f483-47f8-98d3-648bc56fb9ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: w_CTSIB
• Version Model Number: v1.0.4
• Company DUNS: 267153884
• Company Name: VIRTUALIS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760310780302 [Primary]

FDA Product Code

• ISD: Exerciser, Measuring

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-03
• Device Publish Date: 2022-04-25

Devices Manufactured by VIRTUALIS

• 03760310780807 - PhysioVR: 2023-05-12
• 03760310780814 - BalanceVR: 2023-05-12
• 03760310780692 - Motor Control Test: 2022-07-13
• 03760310780760 - MotionVR Research: 2022-07-13
• 03760310780302 - w_CTSIB: 2022-05-03
• 03760310780302 - w_CTSIB: 2022-05-03
• 03760310780555 - StaticVR: 2021-12-17
• 03760310780548 - WalkVR: 2021-12-03
• 03760310780005 - Mirror: 2021-11-29