Bacterial Endotoxin Testing Company believes that data review, cleanliness requirements, microbial contamination level monitoring and automated visual inspection requirements will continue to be the focus of attention in the field as developing countries place increasing emphasis on patient safety and the networking of medical care. Meanwhile, green initiatives will start in the field of medical device packaging as hospitals look to reduce waste. The recyclability of medical packaging materials has been put on the agenda, and a professional medical device material recycling association composed of several companies has also begun to operate. With the development of the times, the improvement of laws and regulations, and the advancement of engineering technology, it is safer and more reliable. Green and recyclable medical packaging materials can fully protect the health and safety of patients and medical workers.

　　The bacterial endotoxin testing company believes that the functions of sterile medical packaging mainly include:

　　(1) Provide microbial barrier and physical protection

　　(2) Must be suitable for sterilization.

　　(3) Keep sterile and intact before use.

　　(4) Easy to open and aseptic transfer.

　　(5) Identify the product and clearly mark the information and warnings.

　　The Bacterial Endotoxin Testing Company believes that for the sterile medical device manufacturing industry, commonly used sterilization packaging materials include porous materials (ie, breathable materials, such as paper and Tyvek) and air-impermeable materials (such as plastic films, etc.). Commonly used packaging forms (sterile and specific pathogen-free) include: hard blister box, soft blister box (FFS packaging), sterile tube bag, plug bag, window bag, etc.

　　Bacterial endotoxin testing companies believe that factors affecting the selection of sterilization packaging materials and packaging design include the specific characteristics of medical devices, expected sterilization methods, intended uses, expiration dates, transportation and storage conditions, etc.

　　Bacterial endotoxin testing company believes that the individual characteristics of medical devices, expected sterilization methods, shelf life, transportation and storage will all affect the design of packaging systems and the selection of materials. As new medical packaging materials continue to enter the medical field and gradually replace traditional cotton packaging materials, they not only improve work efficiency, but also increase the antibacterial effect and change the shelf life of sterile items.

Bacterial endotoxin testing company believes that aseptic packaging (sterile barrier system) is a key and integral part of medical devices, and is the basic guarantee for the safety of sterile medical devices. Let us pay attention together and make unremitting efforts to ensure the safety and effectiveness of medical devices, reduce the occurrence of medical-associated infections, and protect the health of patients and medical staff!

Bacterial endotoxin testing company: The above are some knowledge points about the sterile barrier system. I hope you can study and understand the relevant knowledge carefully, choose the products and equipment that suit your needs, and ensure your own benefits. If you want to know more details, you can contact us Contact us, I believe we can give you a satisfactory answer.