{"id":2373,"date":"2023-05-14T13:35:06","date_gmt":"2023-05-14T11:35:06","guid":{"rendered":"https:\/\/www.yoo.me\/?p=2373"},"modified":"2025-01-29T15:39:59","modified_gmt":"2025-01-29T14:39:59","slug":"entwicklung-fertigung","status":"publish","type":"post","link":"https:\/\/www.yoo.me\/en\/services-en\/entwicklung-fertigung\/","title":{"rendered":"Development & Manufacturing"},"content":{"rendered":"

Mechatronic Medical Engineers<\/a><\/p>\n<\/div>

We provide the development & manufacturing of your medical devices<\/h1><\/div>

In medical engineering, it can be a long way from the initial concept to a ready-to-market serial device.
\nFor this reason, our engineers at Mechatronic Medical Engineers <\/a>not only keep an eye on medical device development, but also constantly optimize the development processes. Whether it is software or electronics development, mechanical designs, verification work or sub-projects in component development – through our networking, with YOOme you are relying on a competent partner.<\/p>\n

The production of medical and in-vitro diagnostic devices is subject to stringent regulatory and documentary requirements for medical device manufacturers. With us, you receive everything from a single source and to the highest quality standards: we transfer your medical device directly to our production site in Germany after development. From there, we deliver devices all over the world. It goes without saying that we meet all the requirements of the standards and guidelines ISO 13485, ISO 9001, FDA, CSA, CCC, Anvisa, UL and VdS, and regular audits confirm our compliance. <\/p>\n<\/div>

Contact us now<\/span><\/a><\/div><\/div><\/div>
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At our production site in H\u00f6hn in the Westerwald region of Germany, we fulfill all requirements of the standards and directives ISO 13485, ISO 9001, FDA, CSA, CCC, Anvisa, UL and VdS.<\/p>\n<\/div><\/div><\/div><\/div>