Izar™

GUDID 03760272650088

Izar™ is intended to rehabilitate hand functions such as dexterous grasp, pinch, and grip, as well as wrist movements in adult patients with hand motor function impairment.

NeuroXtherapeutics SA

Hand dynamometer/pinchmeter, electronic

• Primary Device ID: 03760272650088
• NIH Device Record Key: db031694-2bfb-4a71-afbf-5525e45e70b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Izar™
• Version Model Number: MMIZ-01
• Company DUNS: 486843613
• Company Name: NeuroXtherapeutics SA
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760272650088 [Primary]

FDA Product Code

• JFA: Exerciser, Finger, 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: 2026-03-06
• Device Publish Date: 2023-01-23