Data logging system for medical device monitoring and documentation. Enables comprehensive data capture and compliance with regulatory requirements.
Manufactured by
Eschweiler, Germany
As experienced and liable ODM service provider we develop and manufacture high-tech medical devices in diagnostics, surgery and therapy. Our core competences are: consulting, SW & HW development, project management incl. preparation & evaluation of risk analysis, technical documentation, support for CE marking and FDA approval as well as the fulfillment of the requirements of the EU’s Medical Device Regulation (MDR), contract manufacturing of medical devices from the prototype to the series and worldwide service. According to your demand, we accompany you from the very idea - over the entire life cycle of the product.
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