ScandiDos has attained certification under the European Union Medical Device Regulation (MDR) for its quality system and Delta4 Phantom+ product line. The EU-MDR is one of the world's most robust health tech regulations, and it plays a vital role in ensuring medical devices meet the high standards. The MDR certification aims to enhance the safety and performance of medical devices within the EU, ensuring a high level of protection for patients and users.

It imposes strict requirements on manufacturers regarding medical device design, manufacturing, and testing. Receiving the EU's MDR certification underscores that ScandiDos' products consistently meet the high standards, showcasing dedication to elevating patient safety. The meticulous certification process is a testament to ScandiDos' overarching mission - to lead the industry by delivering cutting-edge solutions that set the benchmark for patient quality assurance (QA).