HandTutor

GUDID 07290019733935

Wearable biofeedback device

MEDITOUCH LTD

Virtual-display rehabilitation system, non-supportive, clinical

• Primary Device ID: 07290019733935
• NIH Device Record Key: acfd6cf0-11d3-4e51-8b5e-929b4402536f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HandTutor
• Version Model Number: HMHT1004R
• Company DUNS: 649792983
• Company Name: MEDITOUCH 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: false
• 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	07290019733935 [Primary]

FDA Product Code

• IOD: Components, Exercise

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: 2023-06-29
• Device Publish Date: 2023-06-21

On-Brand Devices [HandTutor]

• 07290019733997: Wearable movement biofeedback
• 07290019733980: Wearable biofeedback device
• 07290019733973: Wearable biofeedback device
• 07290019733966: Wearable biofeedback device
• 07290019733959: Wearable biofeedback device
• 07290019733942: Wearable biofeedback device
• 07290019733935: Wearable biofeedback device
• 07290019733928: Wearable biofeedback device
• 07290019733911: Wearable biofeedback device
• 07290019733003: Wearable biofeedback device