BYTEC Medizintechnik GmbH

As an ISO 13485-certified company, BYTEC Medizintechnik GmbH has been developing and producing highly innovative medical devices with unique selling points since 1992. In addition to hardware, software and system development, project management is one of the company's core competencies. BYTEC produces devices to the highest quality standards and also provides support in the areas of: Documentation, CE marking, FDA approval and compliance with MDR requirements.

• Product development
• Device production
• Documentation
• Consulting for approval
• Regulatory affairs

• Software, hardware and system development for surgery, therapy and diagnostics
• Production of active medical devices