Hoveround

GUDID 00859781000026

Wheelchair, powered

HOVEROUND CORPORATION

Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible

• Primary Device ID: 00859781000026
• NIH Device Record Key: f05fdb61-333b-4923-baea-d62faef4b6ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hoveround
• Version Model Number: Teknique FWD
• Company DUNS: 789003365
• Company Name: HOVEROUND CORPORATION
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00859781000026 [Primary]

FDA Product Code

• ITI: Wheelchair, 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: 2018-09-10
• Device Publish Date: 2018-08-09

On-Brand Devices [Hoveround]

• 00859781000057: Wheelchair, powered
• 00859781000040: Wheelchair, powered
• 00859781000033: Wheelchair, powered
• 00859781000026: Wheelchair, powered
• 00859781000019: Wheelchair, powered
• 00859781000002: Wheelchair, powered