Jiangsu Changfeng Medical Industry Co., Ltd.

Jiangsu Changfeng Medical Industry Co., Ltd. manufactures medical devices classified under Class A according to regulatory categorisation. While specific product names or categories were not provided, Class A devices typically include low-risk items such as bandages, examination gloves, or simple surgical instruments. The classification reflects their minimal potential risk to patients and users.

The company is headquartered in China, specifically in Jiangsu province. This location is relevant for understanding its operational base and regulatory jurisdiction, though it does not directly impact the classification or approval status of its devices.

Yes, the company’s devices are registered in the eudamed database, which is the EU’s centralised registry for medical devices. Listing in eudamed confirms compliance with European Union regulatory requirements, such as conformity assessment procedures, though it does not imply individual device approval—only that the manufacturer has met EU registration obligations.

The devices manufactured by Jiangsu Changfeng Medical Industry Co., Ltd. fall under Class A classification, which is the lowest risk category in the EU’s Medical Device Regulation (MDR). Class A devices are generally considered to pose minimal risk to patients and users, often requiring less stringent documentation and post-market surveillance compared to higher-risk classes. This classification is determined by factors like the device’s intended purpose and potential harm.