Medical

We design and test the medical devices according to necessary medical software and hardware development standards:

• IEC 60601-1 Medical electrical equipment – Part 1: General requirements for basic safety and essential performance 
• ISO13485 Medical devices quality management system. Requirements for regulatory purposes 
• ISO 14001 Environmental management system 
• ISO 9001 Quality management systems 

• IEC 62304 Medical device software – Software life cycle processes 

These standards are used in our customers' test procedures. In addition, we prepare and make the tests according to the internal standards of individual customers.

Our team of hardware and software experts will help you bring innovation and quality to the healthcare sector, offering a wide range of services including embedded software development and FPGA design.

We have an equipped hardware lab with modern rework stations, allowing us to create precisely tailored solutions for your medical devices.

Beyond development services, we also offer expert testing support, ensuring that your product meets all standards and requirements for medical devices.

• We have developed several FPGA components used in surgery display instruments for our notable customers. The components mutually convert SDI and HDMI video formats and provide image compression. 
• We have supported our important customer in software and hardware testing, i.e., test procedure definition, procedure review, implementation, and execution.

Learn more in our case studies.