As a member of the medical device community, you need access to expert resources and industry knowledge to make critical decisions for your products and patients. We are here to share our expertise and help solve your most complex medical device manufacturing challenges.
A success story demonstrating how our businesses work together to produce technically-challenging, precision components and devices for our customers.
A variety of design variables can impact the overall profile and strength of your pull wire system. We’ll help you better understand your options, so you can make informed decisions for your project.
In this success story, we demonstrate how JunoPacific has partnered and grown with our customer from the design and development phases of their device to the high-volume production they maintain today.
To realize the full benefits of additive manufacturing during all phases of production, it is important to incorporate design for additive manufacturing (DFAM) early in the design process. Optimize your design and manufacturing processes with these tips.
Cretex Medical | CDT offers advanced micro molding solutions by combining high-pressure injection molding, expert design collaboration, material selection, and cutting-edge simulation technologies to achieve precision for features as small as 100 microns.
When it comes to medical device manufacturing, validation is a critical step to ensure compliance, safety, and efficiency. However, it can also be a time-consuming and resource-intensive process. At Cretex Medical | QTS, we understand these challenges and have developed innovative solutions to help streamline your validation process without compromising quality or compliance.
In the realm of medical equipment manufacturing, the design and production of surgical cases and trays demand precision, innovation, and a keen understanding of both medical and ergonomic requirements. At Cretex Medical | rms, we excel in crafting solutions that not only meet but exceed the expectations of our partners in the healthcare industry.
Medical devices on the European market have long been required to display a Conformitè Europëenne (CE) mark, a symbol of conformance, on the labelling to be deemed safe for use. However, now that the United Kingdom (UK) has left the European Union (EU), the regulatory requirements for conformance of medical devices will become more complicated. On July 1st, 2023, EU notified bodies will no longer be recognized in the UK. Likewise, UK notified bodies will no longer be recognized by the EU.
Cretex Medical | rms is one of the largest contract manufacturers of high-quality, tight-tolerance medical devices in the world and operates one of the leading additive manufacturing cells in the U.S. Learn about Cretex Medical | rms’s additive operation from titanium powder to cleaned, finished part in this additive manufacturing video series.
New users of metal additive manufacturing (AM) may not realize nearly everything made via metal AM needs to undergo some degree of heat treatment following the AM process. There are exceptions, but it is usually a good idea to heat treat your products – especially if they are for a demanding application like the medical implants produced at Cretex Medical | rms.