DATATEST DT-200PRO CSSD Steam Sterilization Effect Temperature Verification Instrument: Top Choice in Selangor, Malaysia, Kuala Lumpur (KL), Puchong MTM Precision Sdn Bhd

Description

Brief introduction:

The DT-200PRO CSSD Steam Sterilization Effect Temperature Verifier is a high-temperature, pressure, and moist heat steam sterilization effect monitoring and verification instrument. It is compact, wireless, and features a robust and durable 316 stainless steel casing. It can be used continuously at 150℃ (up to 400℃ with an insulation box). Simple and easy to operate, it is widely used in hospital sterilization supply centers for verifying and recording steam sterilization temperatures. First, identify the most difficult-to-sterilize area (cold spot) in the sterilizer. Then, place the verifier at the cold spot. After sterilization, connect the verifier to a computer. The CSSD Steam Sterilization Effect Temperature Verifier automatically generates a temperature-time curve for that test point throughout the entire sterilization process using dedicated software. Analyzing this curve reveals that if the sterilization requirements are met, the sterilization of other items in the same batch is also considered合格 (qualified/acceptable).

Details:

The CSSD Steam Sterilization Effect Temperature Verifier
DT-200PRO is a high-temperature, pressure, and moist heat steam sterilization effect monitoring and verification instrument. It is compact, wireless, and features a robust and durable 316 stainless steel casing. It can operate continuously at 150℃ (up to 400℃ with an insulation box). Simple and easy to operate, it is widely used in hospital sterilization supply centers for verifying and recording steam sterilization temperatures. First, identify the most difficult-to-sterilize area (cold spot) in the sterilizer. Then, place the verifier at the cold spot. After sterilization, connect the verifier to a computer. The CSSD Steam Sterilization Effect Temperature Verifier automatically generates a temperature-time curve for that test point throughout the entire sterilization process using dedicated software. Analyzing this curve reveals that if the sterilization requirements are met, the sterilization of other items in the same batch is also considered合格 (qualified/acceptable).

The Central Sterile Supply Department (CSSD) of a hospital is responsible for the sterilization, disinfection, and supply of sterile products to all reusable medical instruments, equipment, and supplies across all departments. It is a crucial link in hospital infection control, and the quality of its work is a vital guarantee for medical and patient safety. High-temperature, high-pressure, moist heat steam sterilization is characterized by its strong penetrating power, rapid conduction, reliable action, and safety and convenience, making it the most widely used sterilization method currently.

The Central Sterile Supply Department (CSSD) of a hospital is responsible for the disinfection, sterilization, and supply of sterile products to all reusable medical instruments, equipment, and supplies in all departments of the hospital. It is a crucial link in hospital infection control, and the quality of its work is a vital guarantee for medical and patient safety. High-temperature, pressure, and moist heat steam sterilization is characterized by its strong penetration, rapid conduction, reliable action, and safety and convenience, making it the most widely used sterilization method currently. According to WS 310.3-2009, Part 3 of the Hospital Central Sterile Supply Department's Standard for Monitoring the Effectiveness of Cleaning, Disinfection, and Sterilization, monitoring of pressure steam sterilization requires continuous monitoring and recording of sterilization parameters such as temperature, pressure, and time for each sterilization cycle. Temperature fluctuations should be within +3℃, and the time should meet the minimum sterilization time requirement. Simultaneously, the time, temperature, and pressure values at all critical points should be recorded, and the results should meet the sterilization requirements. The regulations require the establishment of process records for cleaning, disinfection, and sterilization operations, recording the details of each sterilization run, including the sterilization date, sterilizer serial number, batch number, main items loaded, sterilization procedure number, main operating parameters, operator signature, and sterilization quality monitoring results, and archiving these records. These records should be traceable, with cleaning and disinfection monitoring data retained for at least 6 months, and sterilization quality monitoring data and records retained for at least 3 years.

Because sterilization data and records need to be preserved for a long time, chemical and biological monitoring methods cannot meet these requirements well. We must use an independent, wireless recording instrument to automatically record the temperature, humidity, and pressure data throughout the sterilization process. This data is timestamped and can be imported into a computer for statistical analysis, and finally saved in the form of an electronic document.
The temperature-time curve will be saved as an electronic PDF document. Users can easily add annotations such as sterilization date, sterilizer number, batch number, main items loaded, and operator signature to the document. The curve can also be converted into an uneditable report format. The temperature and time data recorded by the validation instrument cannot be modified, accurately reproducing the data changes during the sterilization process.

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