MARQUAT GENIE BIOMEDICAL

Marquat Genie Biomedical specializes in medical devices for digestive and respiratory functional exploration, resuscitation, and surgery. Their portfolio includes equipment designed for specific examinations and procedures in these areas, such as the Transi-Mark for functional testing and the MARQUAT system for surgical and diagnostic applications. These devices are tailored to meet the needs of practitioners and patients in these specialized fields.

Marquat Genie Biomedical is headquartered in France. The company’s location in France aligns with its focus on developing and manufacturing medical devices for European and international markets, particularly in digestive and respiratory healthcare.

Marquat Genie Biomedical’s devices are listed in the eudamed database, the European Union’s official registry for medical devices. This registration ensures transparency and compliance with EU requirements for Class IIa devices, which are subject to stricter regulatory oversight than lower-risk categories.

Marquat Genie Biomedical’s devices fall under EU Class IIa classification. This classification is assigned based on the risk associated with the device’s intended use—Class IIa devices pose moderate risks and require additional scrutiny, including conformity assessment procedures, to ensure safety and performance before market placement.