Movive Education Unit

GUDID 00860001790832

Education Unit for Movive

Medrhythms, Inc.

Neuromuscular rehabilitation software

• Primary Device ID: 00860001790832
• NIH Device Record Key: 57d50a52-0d4f-4f93-923b-70a682fbd213
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Movive Education Unit
• Version Model Number: 005EDU
• Company DUNS: 080565076
• Company Name: Medrhythms, Inc.
• 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: 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	00860001790832 [Primary]

FDA Product Code

• HCC: Device, Biofeedback

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: 2025-06-23
• Device Publish Date: 2025-06-13

Devices Manufactured by Medrhythms, Inc.

• 00860001790825 - InTandem Education Unit: 2025-06-23 Education Unit for InTandem
• 00860001790832 - Movive Education Unit: 2025-06-23Education Unit for Movive
• 00860001790832 - Movive Education Unit: 2025-06-23 Education Unit for Movive
• 00860001790818 - Movive: 2025-03-18 Movive is indicated to support gait rehabilitation and motor function for people living with Parkinson's disease. Movive is inte
• 00860001790801 - InTandem: 2023-11-06 InTandem is indicated to improve walking and ambulation in adult chronic stroke patients. InTandem is intended to be used in the