LiftWalk

GUDID 00860014768613

A non-AC powered mobile patient lifting system

INNOMOTIVE L.L.C

Mobile patient lifting system, manual

• Primary Device ID: 00860014768613
• NIH Device Record Key: 0e5c0ee3-3661-4e4b-97c7-c04f91aa3384
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiftWalk
• Version Model Number: Standard
• Company DUNS: 122432830
• Company Name: INNOMOTIVE L.L.C
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860014768613 [Primary]

FDA Product Code

• FSA: Lift, Patient, Non-Ac-Powered

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: 2026-02-12
• Device Publish Date: 2026-02-04

On-Brand Devices [LiftWalk]

• 00860014768668: Non-AC powered patient lift system.
• 00860014768613: A non-AC powered mobile patient lifting system