186 We adapt documentation to your needs. This means: You describe how you comply with MDR/FDA regulation and we compile the documentation accordingly. Documents of each Device Master File are organized along the process flows linked to the parts list. Therefore, they are available for each instrument at the push of a button. MDR / FDA DOCUMENTATION HAVE IT YOUR WAY Fast access: Documentation and providing the necessary documents becomes easy.
RkJQdWJsaXNoZXIy MzY2NzY=