Because the medical device is one of the government’s focus on fostering export industries,the harmonization of Taiwan UDI Administrative Guidance and the regulations or guidelines around the world can not only reduce the impact from taking forward the UDI policy of medical devices for manufacturers, but also help manufacturers be prepared as soon as possible for UDI specification and labeling in order to sustain their competitiveness.

Simultaneously, it can contribute to the successful follow-up to the Taiwan FDA gradually into domestic UDI Administrative Guidance, achieve the full application of domestic UDI system and improve the quality of care goals.