Kistler Japan G.K. List of Products and Services

The "maXYmos TL ML" is a monitoring system designed for medical device manufacturing processes that collects signals from sensors installed in manufacturing equipment to detect manufacturing defects and foreign matter contamination. Based on clear judgment criteria, management and evaluation for each manufacturing process can be conducted inline, contributing to the prevention of defective products from being released and reducing recall risks. It also includes features that assist with validation, such as the output of documents and audit trails necessary for IQ and OQ, achieving a reduction in project duration. 【Features】 ■ 21 CFR Part 11 certified equipment, widely adopted by overseas medical device manufacturers ■ Switch from visual inspection to detect defective products with higher precision and efficiency ■ Easy operation via a touch panel to set judgment conditions ■ Real-time analysis possible without the need for data organization or processing *In addition to the product catalog, we are currently offering materials that include case studies of overseas implementations. You can view them through "PDF Download." Please feel free to contact us for inquiries.

We introduce an example of how using Kissler's process monitoring monitor maXYmos and press force sensors allows for the measurement of the sliding resistance of syringes, making precise quality control possible by visualizing the load. With maXYmos, it is easy to operate from setting judgment criteria to determining pass or fail using a touch panel.

"maXYmos TL ML" is a process monitoring system that analyzes sensor data obtained on the manufacturing line and automatically determines the quality of each product. It replaces traditional visual inspections, achieving a reduction in inspection labor and uniformity in judgment accuracy. Real-time analysis allows for quick detection of abnormalities and quality management. Designed to comply with FDA regulations, it has a wealth of achievements with overseas medical device manufacturers. It is equipped with validation support features, enabling immediate operation after installation. 【Features】 ■ Certified equipment under 21 CFR Part 11. Widely adopted by overseas medical device manufacturers. ■ Switching from visual inspection allows for more precise and efficient detection of defective products. ■ Easy operation via a touch panel to set judgment criteria. ■ Real-time analysis is possible without the need for data organization or processing. *In addition to the product catalog, we are currently offering materials that include case studies of overseas implementations. You can view them via "PDF Download." Please feel free to contact us with any inquiries.