About us
As an ISO 13485-certified company, BYTEC Medizintechnik GmbH has been developing and producing highly innovative medical devices for other companies since 1992. In addition to hardware, software and system development, project management is one of our core competencies.
We produce devices to the highest quality standards and also provide support in the areas of: Documentation, CE marking, FDA approval as well as the fulfillment of MDR requirements.
Thanks to our newly founded subsidiary BYTEC Legal Manufacturer GmbH, from this year BYTEC will be able to provide everything - whether as a complete package or in part - from a single source: development, market launch, production and market support.