Umitai Medical Technology company have a management  team with a auccessful track record.We are implementing and maintaining the highest industry standards throughout design, development and manufacturing. Our products are manufactured according to the ISO11608-1 standard.All our processes are subject to the medical device guidelines and are certified according to ISO 13485:2003. For Umitai, compliance with this standard means not only implementing a quality system but also ensuring that quality-oriented thinking is a core component of our corporate philosophy.We ensure the lowest possible level of risk through a systematic approach comprising all steps and aspects of device handling, design and manufacturing.For the commercial demand of our customers we manufacture every year hundreds of millions of parts, components, subassemblies and finished products that pose many challenges for quality management. Our quality systems are systematically challenged during numerous audits every year by customers and regulatory authorities. The CFDA on-site audits performed in December 2015, March 2017 did not generate any unqualified items .