embeX develops components and complete devices in medical engineering that conform to the MD Directives 93/42/ECC and 2007/47/EC. Our development process is certiﬁed in accordance with DIN EN ISO 13485, taking into consideration the requirements for medical software in accordance with EN 62304 as well as for risk management in accordance with EN 14971. On request, we complete our developments with certiﬁcation processes (e.g. CE, UL, FDA). We are happy to advise
our customers in detail at every stage of development.