国家药监局批准注册295个医疗器械产品

Core Viewpoint - The National Medical Products Administration (NMPA) approved the registration of 295 medical device products in July 2025, indicating a significant regulatory development in the medical device industry in China [2][3][4]. Summary by Categories Domestic Medical Devices - A total of 240 domestic Class III medical devices were approved for registration, reflecting the growth and innovation within the local medical device sector [2][4]. Imported Medical Devices - The approval included 21 imported Class III medical devices and 29 imported Class II medical devices, highlighting the ongoing integration of international products into the Chinese market [3][4]. Products from Hong Kong, Macau, and Taiwan - Additionally, 5 medical device products from Hong Kong, Macau, and Taiwan were registered, showcasing the regulatory acceptance of products from these regions [3][4].