QUALITY INSPECTION

We’re strictly in accordance with national standards, industry standards and product technical requirements to organize production, strictly in accordance with the Specification, Appendix, QSR820, YY/T 0287-2017 idt ISO 13485:2016 requirements for the Application of Medical Device Quality Management System in Regulations, GB/T 19001-2016 idt ISO 9001:2015 Requirements for Quality Management System to Implement Quality Process Management. 
We have established quality management system to control the life-cycle of tests we provide, including design and development, production, storage and distribution, installation, servicing and final decommissioning and disposal of medical devices. To control all the factors that affect the quality of products, ensure unqualified raw materials are not put into production, unqualified intermediate products are not transferred, and unqualified products are not left factory. 

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