L-Force Oy

L-Force Oy specializes in software applications for radiation information systems. Their products, such as Radu and Radu RIS (various versions), are designed to manage and track radiation therapy and diagnostic imaging records in clinical environments. These tools help log patient data, treatment plans, and equipment usage while ensuring compliance with radiation safety standards.

L-Force Oy is headquartered in Finland and develops its radiation information system software primarily for the European market. Their devices are classified under the EU Medical Device Regulation (MDR) and are registered in the EUDAMED database, demonstrating compliance with EU regulatory requirements for medical software.

L-Force Oy’s devices are listed in the EUDAMED database, which is the official European Union registry for medical devices. This registration reflects their compliance with EU regulatory standards, including classification under the MDR framework.

L-Force Oy’s radiation information system software, including Radu and Radu RIS versions, is classified as Class I medical devices under the EU Medical Device Regulation. This classification applies because the software supports radiation safety and record-keeping functions without posing significant risk to patients, aligning with the lowest risk category for medical software in the EU.