In order to design a reasonable sterilization system for medical devices, the following basic principles must be obeyed:

Packaging is a part of the product. Packaging here refers to "sterile barrier system". The failure of sterile barrier system means the failure of medical devices and products, and the hidden danger may be greater. Because this effect is usually easier to notice or ignore.

External protection packaging system is also very important, but its effectiveness is relatively obvious and will not cause disastrous consequences, so it can not rise to the height of the product. Therefore, for products or designers in the medical device industry, the product itself is a part of the design, so special attention should be paid to the product packaging design.

Due to the particularity of medical devices, the safety of packaging is directly related to the life safety of patients using devices. Of course, some low-end medical device products may not have such serious consequences.

In this life-oriented era, no one can ignore this. Emphasizing the continuous stability of packaging quality is an issue that needs to be considered when the safety of sterilization packaging has been met. In fact, it also meets the requirements of absolute safety of packaging.

For decades, in addition to the quality management system standards designed by the industry at home and abroad, generally speaking. Scientific and strict packaging process confirmation is also a limited method to ensure the continuous and stable packaging quality.