The EU Medical Device Regulation (MDR) requires manufacturers to perform active Post-Market Surveillance (PMS). This means that manufacturers are required to collect and analyse the lifetime data of their devices and upload the data.

However, this requirement can pose intense difficulties for manufacturers whose devices are still largely analogue and depend largely on manual information gathering. CardiLink offers the opportunity to digitise and connect thousands of analogue medical devices in a secure, GDPR- and MDR-compliant manner.  

This contributes to increasing uptime and the availability of medical devices, giving victims of SCA better odds of survival, and potentially saving tens of thousands of lives across the globe annually. It also enables manufacturers to offer their distributors better products, while permitting the latter to offer their customers an improved service concept.