What are production guidelines for sterilization roll?

Most hospitals will set up special disinfection centers, and the sterilization roll plays an important role in ensuring clinical diagnosis and treatment and meeting the needs of medical research. Sterile equipment and dressing packaging, such as sterilization roll, has become an important part of the work of the supply room. It is an indispensable item to ensure the safety and reliability of medical equipment sterilization, effectively control the occurrence of hospital infections, and improve the quality of hospital disinfection.

Here is the content list:

• What criterions should be followed for sterilization roll?

• What is superiority of a sterilization roll pouch meeting standards above?

• Why is it important to comply with the sterilization roll pouch standard?

What criterions should be followed for sterilization roll?

The active ingredients of the sterilization roll must be able to block microorganisms.

In order to protect the contents from contamination by dust and bacteria in the air, the packaging of the sterilization roll must include no damage to the material, complete sealing, appropriate peel strength, and no penetration.

The materials selected for making the sterilization roll must not fall off, so as not to stick to the surgical supplies and taken into the patient's wound.

After the packaging of the sterilization roll is opened, there should be obvious traces showing that it has been opened, and after the packaging is opened, there should be no reseal ability. This is to prevent the sterilization roll package from being opened and contaminated and then closed again.

The opening position and direction of the sterilization roll should be marked, and the opening position should be convenient for the user to open. One side of the sterilization roll should be transparent, so that users can easily identify the surgical supplies inside and access them.

What is superiority of a sterilization roll pouch meeting standards above?

The sterilization roll pouch acts as a sterile barrier after sterilization of medical devices, which plays a role in maintaining the sterility of the devices for a certain period of time, and at the same time sterilizing related accessories of the medical devices. If the sterilization roll pouch is produced according to the above guidelines, then you will find that you get such a product:

The surface is flat and the material is clean.

There is no risk of fiber or wool falling.

The molecular pore size of the material composing the sterilization roll is large enough to ensure that sterilization media such as steam can pass through without obstruction.

The physical properties of the sterilization roll material are good enough, with high toughness and not easy to break, ensuring the integrity of the sterilization process.

Bacteria isolation performance is superior to avoid contamination after sterilization.

Throughout the process of steam and sterilization, the biological load capacity is maintained at an acceptable level.

Why is it important to comply with the sterilization roll pouch standard?

Production according to a certain standard is a very obvious restriction in the eyes of many people, because the establishment of a standard itself means a restriction on products or services. In fact, for industries such as dental sterilization roll pouch, the role of standards is not a limitation.

It just regulates the development of the industry, and hopes that the entire sterilization roll pouch production industry can better serve consumers through relevant standards. With the standard, sterilization roll pouch manufacturers can produce according to the standard, and the related products produced are more in line with market demand.

In a sense, the standard does have a restriction, but for the entire sterilization roll industry, this restriction can help the survival of the fittest in the sterilization roll industry. The competition among sterilization roll companies is very fierce. If there is no standard, the competition will have no bottom line, which will eventually affect the development of the entire industry.

The standard of sterilization roll pouch is the foundation of innovation in this industry, and innovation based on this foundation is meaningful. The national standard is a reference to the sterilization roll pouch. When producing, the standard can ensure the quality of the production. Only when the quality of the sterilization roll pouch is ensured, can innovation be discussed.

The market segment of sterilization roll is relatively small, and companies need to continuously extend their product lines to get rid of the growth restrictions of single segment life cycles. Hefei Hanchin adheres to the sterilization roll production standard line, and continuously innovates on the basis of meeting quality requirements to meet consumer needs.