Armotion

GUDID 07640174420025

Robotic assisted device for the rehabilitation of the upper extremity

Reha Technology AG

Virtual-display rehabilitation system, powered-support

• Primary Device ID: 07640174420025
• NIH Device Record Key: 8cf01e8b-bb23-4588-98ed-b6ac1177babb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Armotion
• Version Model Number: Armotion
• Company DUNS: 486234078
• Company Name: Reha Technology AG
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640174420025 [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: 2018-03-29
• Device Publish Date: 2016-10-06

Devices Manufactured by Reha Technology AG

• 07640174420032 - G-EO: 2020-05-06 Robotic-assisted gait trainer
• 07640174420018 - G-EO System: 2020-05-06 Robotic-assisted gait trainer
• 07640174420025 - Armotion: 2018-03-29Robotic assisted device for the rehabilitation of the upper extremity
• 07640174420025 - Armotion: 2018-03-29 Robotic assisted device for the rehabilitation of the upper extremity