1, the need for regulatory compliance: medical devices, as a kind of food and drug, need to be managed and regulated in strict accordance with national regulations and standards during the production process. Disclosure of raw material components can reduce or avoid the use of poor quality or smuggled raw materials, to force device manufacturers to strictly comply with the production norms, to prevent the use of raw materials that may pose a risk to human health, so as to ensure the safety, efficacy and quality of the product.
2, the need for information transparency: In addition, the public disclosure of raw material components also help to increase the transparency of information on medical devices, to facilitate consumers to understand product quality and utility. Consumers can view the raw material components of the product, further understanding of the product manufacturing process, product characteristics, the use of the effect and other related information, which is conducive to consumers to make a more informed choice when buying.