Power Wheelchair

GUDID 06978949461333

Zhejiang Innuovo Rehabilitation Devices Co., Ltd

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06978949461333
• NIH Device Record Key: cd263e89-7938-4e79-92b1-5b57a96d16ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Power Wheelchair
• 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	06978949461333 [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: 2025-08-18
• Device Publish Date: 2025-08-09

On-Brand Devices [Power Wheelchair]

• 06970765972246: N5909
• 06978949462248: N5909
• 06978949461333: W5907(Q50 R Carbon)
• 06978949462231: W5213
• 06978949460916: N5513A
• 06978949461531: W5213
• 06978949461517: N5513A
• 06978949461456: W5521
• 06978949461449: W5213
• 06978949461036: N5513A
• 06978949461012: N5513A
• 06978949460978: N5513A