EURORAD 2-6

UURORAD 2-6 specializes in semiconductor radiation detectors, including the EUROPROBE series. These devices are engineered for precise radiation detection and imaging, serving both medical and industrial applications. The company focuses on developing systems from high-purity semiconductor materials to complete detection solutions.

UURORAD 2-6 is based in France. Its devices fall under the EU’s medical device classification system, specifically Class IIa, which applies to devices posing a low to moderate risk. This classification requires compliance with EU regulatory requirements, including conformity assessment procedures and registration in the EU’s eudamed database.

Yes, EURORAD 2-6’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and compliance with EU regulatory obligations for Class IIa devices, allowing healthcare professionals and authorities to verify the device’s legal status and manufacturer details.

UURORAD 2-6’s devices are classified as Class IIa under the EU Medical Device Regulation (MDR). This classification is determined by factors such as the device’s intended purpose, potential risks, and the level of intervention it involves. Class IIa devices require a higher level of scrutiny than Class I but less than higher-risk classes, ensuring they meet strict safety and performance standards before market placement.