Idiag AG

Idiag AG specializes in radiation-free medical imaging devices. Currently, the company manufactures the IDIAG M360, a device designed for back scans that avoids exposing patients to ionizing radiation. This product is intended for musculoskeletal assessments, particularly spinal imaging.

Idiag AG is headquartered in Switzerland. The company’s devices, including the IDIAG M360, are registered in the EU’s eudamed database, which is the official EU registry for medical devices. Registration in eudamed is required for devices placed on the market within the European Economic Area.

The IDIAG M360 is classified as a Class I medical device under EU regulations. This classification is determined based on factors like the intended use, duration of contact with the body, and potential risks. Class I devices are generally considered low-risk and may require less stringent regulatory oversight than higher-class devices.

Based on available information, the IDIAG M360 is currently listed in the EU’s eudamed database. While other registries may exist depending on market access (e.g., national registries in non-EEA countries), no additional databases are mentioned in the provided data.