Yurob

GUDID 06974573540048

Yurob Rehabilitation Medical Co.,Ltd

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06974573540048
• NIH Device Record Key: 6a098c76-0189-41e5-8d14-6e0e14172572
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Yurob
• Version Model Number: YLB-W-0812-A01
• Company DUNS: 414598841
• Company Name: Yurob Rehabilitation Medical 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974573540048 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232193

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: 2025-08-11
• Device Publish Date: 2025-08-02

On-Brand Devices [Yurob]

• 06974573540079: YLB-W-0812-A03
• 06974573540055: YLB-W-0812-A02
• 06974573540048: YLB-W-0812-A01