REOGO REOGO005SYS

GUDID 07290017844107

The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients with motor limitations, recovering from CVA or other neuromuscular conditions. The Motorika ReoGo™ System is rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints specifically designed to prevent the adhesion and contracture of joints, to improve the patients’ range of motion and functional capabilities of the upper extremity.

MOTORIKA MEDICAL (ISRAEL) LTD

Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb Virtual-display rehabilitation system, powered-support, upper-limb

• Primary Device ID: 07290017844107
• NIH Device Record Key: 8877a4e7-6278-41a3-a9ba-2456c7e87247
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REOGO
• Version Model Number: 08
• Catalog Number: REOGO005SYS
• Company DUNS: 534078621
• Company Name: MOTORIKA MEDICAL (ISRAEL) LTD
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290017844107 [Primary]

FDA Product Code

• IKK: System, Isokinetic Testing And Evaluation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-08-05
• Device Publish Date: 2019-05-31

On-Brand Devices [REOGO]

• 07290017844114: The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients wit
• 07290017844107: The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients wit