INNUOVO

GUDID 06970765971331

Zhejiang Innuovo Rehabilitation Devices Co., Ltd

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06970765971331
• NIH Device Record Key: f83ba80c-8ff7-4ba1-a888-5f3ba5a72d89
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INNUOVO
• Version Model Number: W5907(Q50 R Carbon)
• Company DUNS: 544392592
• Company Name: Zhejiang Innuovo Rehabilitation Devices Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970765971331 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220740

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: 2024-04-02
• Device Publish Date: 2024-03-25

On-Brand Devices [INNUOVO]

• 06970765970914: N5513A-091
• 06970765971331: W5907(Q50 R Carbon)
• 06970765972239: W5213
• 06970765972222: W3467
• 06970765972215: W3467
• 06970765972208: W3331
• 06970765972192: W3331
• 06970765972185: W3431
• 06970765972178: W3431