OmniTour System

GUDID 00858703006382

Interactive cycling therapy feedback device.

ACCELERATED CARE PLUS CORP

Virtual-display rehabilitation system, non-supportive, clinical

• Primary Device ID: 00858703006382
• NIH Device Record Key: f7971ade-85c1-492b-a250-d27de87e31f3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OmniTour System
• Version Model Number: 300800T
• Company DUNS: 828331616
• Company Name: ACCELERATED CARE PLUS CORP
• 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com
• Phone: 800-350-1100
• Email: acp-customersupport@hanger.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858703006382 [Primary]

FDA Product Code

• ION: Exerciser, Non-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: 2024-09-18
• Device Publish Date: 2024-09-10

Devices Manufactured by ACCELERATED CARE PLUS CORP

• 00858703006399 - OmniCycle Elite 7 Inch Screen Motorized Therapeutic Exercise System: 2024-10-29 Motorized therapy cycle with a 7 inch screen that can connect to the OmniTour system
• 00858703006382 - OmniTour System: 2024-09-18Interactive cycling therapy feedback device.
• 00858703006382 - OmniTour System: 2024-09-18 Interactive cycling therapy feedback device.
• 00858703006375 - OmniTour: 2023-12-04 Therapy cycling feedback software
• 00858703006313 - OmniFlow Software: 2023-09-14 Respiratory assessment and exercise software
• B179OMNI13E87E4 - OmnisEMG: 2023-09-14 Biomechanical function analysis / interactive rehabilitation system
• 00858703006337 - Synchrony Dysphagia Solutions by ACP: 2023-09-11 Bioelectrical signal analysis software; Biomechanical function analysis, interactive rehabilitation system
• 00858703006351 - OmniVR Elite: 2023-09-11 Virtual display rehabilitation system
• 04041925002799 - OmniCycle Elite: 2023-09-11 Powered exercise therapy bicycle