Congratulations！
Suzhou Acmed has successfully completed the second surveillance audit under the European Union Medical Device Regulation (MDR), further demonstrating the effectiveness of its quality management system and commitment to regulatory compliance.
The successful completion of the audit reflects the company’s ongoing efforts to maintain high standards in quality management and operational excellence. It also reinforces Acmed’s ability to provide safe, reliable, and compliant medical products to customers and partners worldwide.
Looking ahead, Suzhou Acmed will continue to focus on continuous improvement, quality excellence, and customer satisfaction, while further strengthening its compliance capabilities to support sustainable growth in the global healthcare market.