ZENO ELECTRONIC WALKWAY ALL SIZES

GUDID 00860252000704

The Zeno Electronic Walkway with PKMAS Software deliver Gait Analysis measurements that describe the performance, style, effectiveness and efficiency of walking without referring to its etiology.

Zenometrics LLC

Gait analysis system

• Primary Device ID: 00860252000704
• NIH Device Record Key: 8146c533-1e42-4900-854d-8bac76dae0fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ZENO ELECTRONIC WALKWAY
• Version Model Number: Platinum
• Catalog Number: ALL SIZES
• Company DUNS: 028456795
• Company Name: Zenometrics LLC
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com
• Phone: 914-263-5987
• Email: info@zenometrics.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860252000704 [Primary]

FDA Product Code

• JFC: System, Pressure Measurement, Intermittent

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: 2021-02-16
• Device Publish Date: 2021-02-08