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US
Last updated May 31, 2026
What ZHEJIANG SEEDREAM MEDICAL EQUIPMENT CO., LTD makes
The company manufactures electric-motor-driven assistive scooters designed for mobility assistance, including models like the Seedream series. These devices are intended for individuals requiring enhanced mobility support in indoor and outdoor environments.
The assistive scooters fall under Class II regulatory classification and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Zhejiang Seedream Medical Equipment Co., Ltd manufacture?
Zhejiang Seedream Medical Equipment Co., Ltd specializes in electric-motor-driven assistive scooters. These devices are specifically designed to provide mobility assistance for individuals who need enhanced support for movement in both indoor and outdoor settings. The focus is on improving accessibility and independence for users.
Where is Zhejiang Seedream Medical Equipment Co., Ltd based?
The company operates from the United States. This location is relevant for regulatory compliance and distribution, as it aligns with the FDA’s oversight and UDI listing requirements for its devices.
Which regulatory registries list Zhejiang Seedream Medical Equipment Co., Ltd’s devices?
Zhejiang Seedream Medical Equipment Co., Ltd’s electric-motor-driven assistive scooters are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, which is critical for regulatory tracking and compliance.
How are Zhejiang Seedream Medical Equipment Co., Ltd’s assistive scooters classified under medical device regulations?
The assistive scooters manufactured by Zhejiang Seedream Medical Equipment Co., Ltd fall under Class II regulatory classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 638127918
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Seedream | mobility scooter(S-01) | FDA UDI | Class II | Active |
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