Do You Know The Importance Of Continuous Band Sealer Performance Verification?

The normal operation of the equipment in the disinfection supply center is a prerequisite for ensuring the quality of sterilization. With the implementation of the Ministry of Health "Hospital Disinfection Supply Center Management Regulations", the disinfection supply center is constantly updating and configuring advanced cleaning, disinfection, and sterilization equipment , There are also new regulations on the monitoring of equipment operation effects in the specification. The staff are familiar with the operation of various equipment and strengthen daily maintenance and safety management training.

The continuous band sealer, often used in daily work, its sealing function is to prevent microorganisms from entering the inside of the sterilized packaging material, thereby ensuring the sterile state of the packaging. In order to achieve this goal, it is particularly important to safely and reliably meet the sealing process of the series of specifications.

The sealing process can only guarantee its safety through correct operation. The defects in the sealing area are usually difficult to observe with the naked eye, and the operator must eliminate various other unsafe factors. In order to ultimately ensure the safety of the patient, it is of great significance to monitor the key parameters during the entire sealing process. The sealing process must meet the requirements of scientific and technological development, as well as the requirements of relevant specifications, directives and regulations for medical devices.

Sealing performance verification needs to be completed by the equipment user, and the verification process must use a certified method that meets the relevant specifications. In order to ensure the normal progress of the sealing process, the sealing equipment should first be able to work correctly. The manufacturer of the continuous band sealer, equipment is obliged to guide and train users on how to perform the correct sealing operation, and must ensure that each user who uses the sealing equipment can use the equipment correctly and safely. The user must be able to correctly master the monitoring of the key parameters of the sealing equipment, including temperature, pressure, sealing speed and time.

The supplier of medical packaging materials must ensure that the products provided are compatible with the key parameters of the sealing equipment, and at the same time need to instruct users on how to store medical packaging materials. Storage conditions that do not meet the standard will usually cause the paper-plastic packaging materials to expand and deform, and small leaks will occur during sealing. The product quality and storage conditions of medical packaging materials need to be consistent with the requirements of relevant specifications, which are the prerequisites for the atmosphere to ensure the safety of the sealing process.

The user is obliged to perform regular maintenance on the continuous band sealer, and to verify the sealing performance once a year to ensure the safety of the sealing product. Generally speaking, only relying on visual observation will miss many actual defects in the sealing area, which may lead to the failure of the sterile barrier system. Therefore, it is very necessary to use professional testing methods that meet relevant standards. Many users trust the sealing equipment too much and neglect the regular sealing performance verification. In the process of regular testing, sealing equipment and medical packaging materials need to be verified in accordance with relevant requirements.

In order to make the equipment of the disinfection supply center play a good role, extend their service life, increase the utilization rate of the equipment, and ensure that the quality of cleaning, disinfection and sterilization is efficient and fast, the safety management and daily maintenance of the equipment of the disinfection supply center are essential.