Motion Trainer

GUDID 00196852042524

Trainer Rx, Inc. D/B/A Recoveryone

Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use Virtual-display rehabilitation system, non-supportive, home-use

• Primary Device ID: 00196852042524
• NIH Device Record Key: 362c5b42-e5e3-4169-8825-26839b72ef1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Motion Trainer
• Version Model Number: 2.22
• Company DUNS: 062312936
• Company Name: Trainer Rx, Inc. D/B/A Recoveryone
• 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	00196852042524 [Primary]

FDA Product Code

• QKC: Interactive Rehabilitation Exercise Device, Prescription Use

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: 2023-09-06
• Device Publish Date: 2023-08-29