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Tackle MDR requirements with your supplier’s material expertise
The EU medical device regulation (MDR) 2017/745 was announced five years ago and will fully apply on May 26, 2021. The new MDR poses major challenges for medical device manufacturers. Through close cooperation, suppliers can support medical device manufacturers in complying with these requirements.
Understanding Molding Complexity to Reduce Device Complexity
As medical devices become ever more sophisticated and smaller in size, component manufacturers must adapt manufacturing processes to fit multiple functions into a limited space. A means of addressing this challenge comes in the form of multi-component Liquid Silicone Rubber (LSR) technology, which provides designers with the latitude and flexibility to enhance their applications. Learn how multi-component LSR technology can support medical devices.
Case studies in applying advanced extrusion technologies for medical device design
Geometric transition extrusion manufactured of HCR silicone support medical devices engineers in their efforts to design smaller, more intricate and complicated medical devices and at the same time, comply with increasingly stringent national and international regulations.
This webinar goes through the advanced extrusion process and takes a look at several case studies demonstrating how this process can be used in the manufacture of components for innovative medical devices.
Solving Complex Device Design Challenges through Partnership
This webinar reviews the benefits of partnering with experts in molding and extrusion to optimize medical device design and eliminate challenges before they happen, leading to a faster prototyping timeline and a higher quality device.
Expert pieces on seals and engineered products - Our collection of technical articles highlights a range of sealing technology topics. Trelleborg Healthcare & Medical experts share their insights on the latest advances in seals and engineered products.