Zhejiang Dreamotion Technology Co., Ltd.

Zhejiang Dreamotion Technology Co., Ltd. specializes in electrically powered assistive devices for patient care. Their primary products include electrical assistive beds, such as the *Dreamotion home-care bed*, which are designed for adjustable support and comfort in home settings. They also produce patient lifting system toilet seats, like the *Jiecang toilet lift*, which help individuals with mobility limitations transfer safely to and from toilets.

The company, Zhejiang Dreamotion Technology Co., Ltd., has a presence in the United States, though its headquarters are based in China. While the company operates in the U.S. market, regulatory oversight for its devices—such as compliance with FDA requirements—applies to individual products, not the company itself.

Zhejiang Dreamotion Technology Co., Ltd.’s devices are classified as Class II medical devices. This classification is determined by regulatory authorities based on factors like the device’s intended use, potential risks, and the level of oversight required for patient safety. Class II devices typically undergo special controls beyond general controls to ensure their safety and effectiveness.

Yes, Zhejiang Dreamotion Technology Co., Ltd.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product identifier to medical devices to improve tracking, reduce medical errors, and enhance transparency in the healthcare system. Listing in this registry helps healthcare providers and regulators verify device details, such as manufacturer information and regulatory status.