ISO 13485 certification is an international standard for the medical device industry worldwide. This certification emphasizes the establishment and maintenance of a quality management system, aiming to ensure that products meet the rigorous requirements of the medical industry and consistently provide high-quality, safe, and reliable medical devices.
By complying with the ISO 13485 standard, the company ensures comprehensive control from product design to production, sales, and after-sales service, meeting needs for reliability and effectiveness.
As a national high-tech enterprise and a technology-based company, we take pride in being recognized as an honest enterprise and a member of the excellent domestic medical product catalog.
Since 2006, the focus has been on innovative development and manufacturing of ultrasound imaging, digital electrocardiograph, and digital radiology imaging products. The product portfolio consists of over 50 models in five major categories, including full digital color Doppler ultrasound diagnostic systems, patient monitors, and digital radiography equipment.
With three technology research and development centers and more than 100 product technology patents, we possess independent intellectual property rights and maintain a global perspective to serve medical professionals worldwide.
Our dedicated team works closely with customers to ensure satisfaction. Whether it's technical support during product usage or any post-sales service requirements, we provide comprehensive assistance.
Technical experts with extensive knowledge are capable of responding promptly and resolving issues efficiently. We offer remote technical support through phone, email, or remote assistance tools to assist with equipment operation, troubleshooting, and software issues. Detailed product user manuals and technical documents are provided for reference at any time.