Seedream

GUDID 06978388998889

ZHEJIANG SEEDREAM MEDICAL EQUIPMENT CO.,LTD

Assistive scooter, electric-motor-driven

• Primary Device ID: 06978388998889
• NIH Device Record Key: 5c108e2c-a4ef-4b74-8673-0911012a981b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Seedream
• Version Model Number: mobility scooter(S-01)
• Company DUNS: 638127918
• Company Name: ZHEJIANG SEEDREAM MEDICAL EQUIPMENT 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: false
• 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	06978388998889 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242714

FDA Product Code

• INI: Vehicle, Motorized 3-Wheeled

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: 2025-04-10
• Device Publish Date: 2025-04-02