TYMO

GUDID 09120077180045

The TYMO system is a modern monitoring and therapy device for the rehabilitation of patients suffering from motoric dysfunctions; it is primarily used for neurological rehabilitation purposes.

tyromotion GmbH

Virtual-display rehabilitation system, non-supportive, clinical

• Primary Device ID: 09120077180045
• NIH Device Record Key: b86122d0-badb-466a-84bc-e50ab55b967f
• Commercial Distribution Discontinuation: 2026-03-12
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: TYMO
• Version Model Number: 5
• Company DUNS: 301726803
• Company Name: tyromotion GmbH
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	09120077180045 [Primary]

FDA Product Code

• BXB: Exerciser, Powered

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: 2026-03-13
• Device Publish Date: 2022-09-18

On-Brand Devices [TYMO ]

• 09120077180144: TYMO is a monitoring and therapy device for the rehabilitation of patients suffering from motori
• 09120077180045: The TYMO system is a modern monitoring and therapy device for the rehabilitation of patients suf