Medical devices are a group of products intended for diagnosis, treatment, prevention, or the supplementation/replacement of bodily functions. Because they concern human life, extremely high levels of safety, reliability, and quality, compliant with the Pharmaceuticals and Medical Devices Act (PMD Act) and ISO 13485, are required. They encompass a wide range of products such as CT scanners, MRI machines, surgical assistance robots, artificial organs, and diagnostic equipment, integrating technologies like precision machining, biocompatible materials, advanced software development, and sterilization. In the manufacturing process, the establishment and operation of a rigorous Quality Management System (QMS) and validation are indispensable. Furthermore, maintenance and servicing throughout the entire product lifecycle, as well as PMD Act compliance consulting, are also important service areas. It can be said that this is a field where technological innovation and regulatory compliance are constantly required.