Medical devices generally experience R & D certification stage, small batch stage, high-volume stage, the requirements of suppliers are not the same, so first of all, the medical device supplier requirements are very high, the need for them to have a very strong development capabilities, very good quality control capabilities, and at the same time, due to the specificity of the medical industry, but also need to be very deep understanding of the medical industry by the medical industry to meet the requirements of the company will be basically a large and medium-sized companies, the company will be the first to meet the requirements of the medical industry. Requirements of the company will be basically large and medium-sized parts supporting enterprises.
Medical devices in the research and development stage, high requirements, the number of small, most of the small and micro-enterprises are difficult to pay the high cost of research and development, and product certification cycle is very long, into mass production may take 2-5 years, so destined to large enterprises are not willing to cooperate, only those in the survival of the pressure on the small enterprises are willing to take over this kind of business, resulting in the current status of the medical parts supplier: small size, weak, single product category, and the medical industry is a good quality control capability. The current situation of medical parts suppliers: small enterprise scale, weak strength, single product category, incomplete quality system.