We are YOOme
UID expands its portfolio in the field of medical technology: We are YOOme! Five strong experts have united under this name: BAYOOCARE, BAYOOMED, Mechatronic, Puls Produktdesign and UID. In addition to user experience design, we now offer our customers in the medical sector a wide range of new services, such as device development and manufacturing as well as international approval and marketing.
YOOme accompanies customers in their challenges around medical devices: From the first idea, concepts, design, visualization, development, certification, reliable manufacturing to post-market surveillance. For all your needs and questions, a YOOme contact person is available, who coordinates and manages the five experienced and well-connected medical technology companies operating in the background. All YOOme partners are part of the BAYOONET Group.
The offer is particularly interesting for existing UID customers from the medical technology sector. Because here we can now provide support in significantly more areas.
Will we meet at MedtecLIVE?
At MedtecLIVE with T4M from May 23-25, 2023 in Nuremberg, we will inform you about our expanded range of products. Visit us in hall 1, booth 1-404 and convince yourself of the YOOme portfolio. Make an appointment with our experts now and get a free ticket.
The YOOme services at a glance
You do not have an idea yet, but would like to already future-proof your company with innovative products? Our experts will help you. By utilising innovation methods, feasibility studies and market analyses we support you on your way. And in case you already got an idea, we are more than happy to test it for practicability.
We plan and develop a concept for you meeting all requirements concerning compliance, product design, usability as well as system and safety specifications. We are also happy to handle the application for inspection by the Notified Body.
We design and engineer software and hardware for your medical device while keeping UX, UI and industry design in mind and even creating formative studies along the way. Always being on top of all regulatory requirements seems impossible to you? No problem at all. As legal manufacturer or consultant we take care of all of your regulatory affairs.
By means of automated test procedures, we check and verifiy your hardware and software for usability duration and system errors. We also do a summative study of your medical device pre-launch.
A successful approval is not the end of the product life cycle: We will support your post-market surveillance and vigilance. Or as support for questions concerning sofware, marketing or a product - even for cloud requests we are happy to help.