CEA Medical Manufacturing has over 25 years of medical device experience obtained from serving the world’s top medical OEM’s. A partnership with CEA is the instant acquisition of over two decades worth of medical device development and manufacturing experience.
Our engineering experience, resources and talent provides for an effective evaluation of a device’s design, materials, and components. By doing so, our Engineering Team proactively identifies issues and solutions from concept through production ensuring a successful product launch, continued production fulfillment and uncovering cost savings.
CEA Medical Manufacturuing combines state-of-the-art engineering tools with six sigma for design methods. Our customers have simultaneous access to engineers with degrees in electrical, mechanical,microbiology, industrial, plastics, quality, and manufacturing engineering. Our engineers can turn our customer's concepts and requirements into fully engineered designs, or provide their engineers with valuable feedback on the manufacturability of their designs. Either way our customers end up with a product that can be efficiently manufactured.
Partial List of Engineering Tools:
We develop ideas, concepts or detailed designs into products that not only meet the original requirements, but also offer optimized manufacturing solutions. Our expertise in risk analysis; design verification; tool and fixture fabrication; process development; and process validation; makes us the ideal partner for speedy product development. CEA maintains a highly productive strategy to continually improve and lean-out the manufacturing process through development and into production transfer.
Our skilled engineering staff has many years of experience in transitioning engineered designs to manufactured devices. They are equally equipped to evaluate and transfer existing manufacturing lines or assembly processes. Our methods include: a thorough review and transfer of your documentation; executing process characterizations and improvements; facilitating component qualifications, and equipment and tooling IQs; performing OQs and PQs; and managing re-validation of packaging and sterilization.