Medical Technology


Digitization opens up a wide range of new possibilities in medical technology. The range of functions of medical devices can be expanded and improved. Additionally, purely digital products such as health apps have also become possible. Hardware components of many medical devices or medical technology equipment are increasingly being supplemented by software and linked-up digitally. Secure and reliable communication between medical devices has become indispensable in almost all areas of application.
A key advantage of this development is cost-effective maintenance and further development of medical devices. Now, error data can be recorded, smaller maintenance procedures can be triggered and software updates can be carried out. Here Navimatix comes into play:

With our experience as software developers in the medical technology industry as well as in the fields of connected devices and edge computing, we accompany your company throughout the whole process: from idea to subsequent developments to completion of your product or device.

Digital Solutions in Medical Technology

To implement your requirements, we at Navimatix use methods like agile project management, staying focused and resource-conscious up to a successful release and beyond:
  • Consulting
  • Conceptual Design
  • Development
  • Product Management
  • Service
  • Further Development
This allows us to tailor your product to the exact needs of your customers and yourself.

Medical Devices Regulation

We are the helping hand to develop your medical devices together with you in a competent and standard-compliant way. We support you in complying with all relevant normative and regulatory requirements of the Medical Devices Ordinance:

  • Agile software development compliant with regulatory framework (AAMI TIR45)
  • Short communication channels allow a quick implementation of your requirements and wishes
  • Short-term realization of necessary adjustments
  • Engineering according to IEC 62304, IEC 62366 und ISO 14971
  • Embedding in your existing quality management system according to DIN EN ISO 13485

We will be happy to advise you.

Dr. Florian Rasche
Project Manager

+49 3641 32799-39

Do you have questions about software development according to the European Medical Device Regulation (MDR)?

Contact us, we will be happy to support you in implementing them in your project!

You have the requirement, we have the smart tools. Together, we launch a successful, competitive medical technology product.

A new project?
We are curious.

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