ISO 13485 is the international standard for the medical device industry. This certification ensures that our quality management system meets rigorous requirements for design, production, and after-sales service.
Our commitment to quality means we consistently provide high-quality, safe, and reliable medical devices to healthcare professionals worldwide. We strictly follow CFDA and European CE quality standards.
Our company is a national high-tech enterprise and a technology-based medical device manufacturer. Since 2006, we have been dedicated to the innovation and manufacturing of ultrasound imaging, digital electrocardiographs, and radiology products.
We operate multiple technology research and development centers and hold more than 100 technology patents. With a global perspective, our marketing and service network reaches customers in more than 100 countries and regions, benefiting nearly 100,000 medical professionals.


Our dedicated service team consists of experienced technical experts capable of providing prompt assistance. We offer remote technical support via phone or email for troubleshooting, software updates, and operation guidance.
In addition to remote support, we provide on-site repair services and maintain a comprehensive stock of spare parts to ensure your equipment returns to operation as quickly as possible.