What are the requirements for the sterilization roll?

The definition of the sterilization flat roll should be understood as packaging for medical device products, sterilization, aseptic operation (such as clean opening), acceptable microbial barrier performance, Packaging systems that protect products before and after sterilization and maintain a sterile environment within the system within a certain period. Because this concept usually does not include the outer protective sterilization flat roll system (buffer packaging and assembly packaging, etc.), the package system can also be called an "aseptic barrier system ".

Here is the content list:

•Prevent bacteria from entering

•Absolute packaging safety

•Through rays

Prevent bacteria from entering

Sterilization gas etc sterilization factor size & it; envelope pore size & it; bacterial size, sterilization packaging material through sterilization factors (such as ETO ethylene oxide, high-temperature steam, gamma cobalt 6 0 rays, etc .) but is blocked semi-permeable to bacteria. Establish an "aseptic barrier system ", because the failure of the aseptic barrier system means that the medical device product fails, and the hidden risk is likely to be greater because this failure is usually less detectable or more easily ignored. Therefore, for the product development or technical designers in the medical device industry, we should pay special attention to this point and focus on the packaging design of the product, because this is also part of the product's design.

Absolute packaging safety

As for the emphasis on the continuous stability of the packaging quality, this is the problem that should be considered next under the big premise of the safety of the sterilization flat roll. This is also a requirement to meet the absolute safety of the packaging. Generally speaking, scientific and strict packaging process confirmation is also an effective method to ensure continuous and stable packaging quality. For example, the sterilization flat roll of Hefei Hanchin Company.

Through rays

The radiation is sterilized through the sterilization flat roll, and finally, the bacteria can not get in (because the pore size of the packaging material is semi-permeable, allowing sterilizing gas, rays in and out, but preventing bacteria) is the use of the bag's choice of semi-permeable dialysis, which ensures that the medical equipment in the package is sterile after sterilization, before handling, transporting, and storing until the nurse in the hospital operating room opens.

Medical sterilization flat roll is to prevent the goods in the bag from being contaminated by bacteria, generally, in a completely closed form, bacteria can not enter to achieve its effect. A medical device is packed into a sterilization flat roll (product), then sealed, sterilized, and sterilized, using the sterilization flat roll (product) to pass through the sterilization factor, not through the semi-permeable permeability of bacteria. After the professional examination of EN868 by Suzhou University Medical Laboratory, the packaging bag (product) can reach several years. Hefei Hanchin company conducts many tests of sterilization flat roll, and the quality qualification rate is guaranteed. If you need a sterilization flat roll, you can consider our cost-effective products. Hefei Hanchin company's materials are non-toxic and tasteless, perfect after-sales service, you can have no worries.