NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD.

GUDID 06975028630628

Ningbo Youhuan Automation Technology Co., Ltd

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06975028630628
• NIH Device Record Key: 8de23e7f-6af2-4b20-9965-b53fbf39a9c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD.
• Version Model Number: artemis
• Company DUNS: 709462082
• Company Name: Ningbo Youhuan Automation Technology 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	06975028630628 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240638

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: 2025-03-04
• Device Publish Date: 2025-02-24

On-Brand Devices [NINGBO YOUHUAN AUTOMATION TECHNOLOGY CO., LTD.]

• 06975028630628: artemis
• 06975028630529: artemis pro