From Your Idea to Market Success
Our core competence is the efficient contract development and production of technically demanding or high-risk medical devices in the areas of diagnostics, surgery and therapy.
We support you as a certified service provider for the CE marking, FDA approval and the fulfillment of the requirements of the EU’s Medical Device Regulation (MDR).
And even during series production, we ensure that your product is the best solution for your customers – by continuing to develop it with you, updating the software, providing on-site service worldwide as well as long-term spare parts logistics.
Your Demand: Our Services
Take advantage of our profound expertise and enthusiasm for medical technology. Together with you, we work out the optimal specifications, create a requirement-oriented design and develop your project in time to market.Find out how
Build upon our responsibility for the entire manufacturing process. Our lean production achieves maximum precision with maximum efficiency – from pilot series to series production.Find out how
Rely upon our service technicians and their expertise in medical devices. You enjoy a prompt and worldwide repair and maintenance service.Find out how
Benefit from our many years of experience in all lifecycles of your medical device – from the feasibility check to topics on regulatory affairs and approval to after-sales support.Find out how
You have an idea and only need the right support?
Then let’s talk. Together we will find out what your project needs. Whether it’s a complete product development or a service within your established process – we are qualified to help you.
BYTEC has been working in the field of in vitro diagnostics (IVD) and life science research (LSR) for several years ... see more ›See all news