Exo'Mouv

Exo'Mouv specializes in wearable compression garments for medical use, including the Exo'Shirt and Abdo'Shirt lines. These garments are designed to provide targeted compression support during post-surgical or post-traumatic recovery. The Exo'Shirt series focuses on the thoracic and upper abdominal regions, while the Abdo'Shirt series targets the lower abdomen and pelvic area. Each product is tailored to specific anatomical zones for clinical applications.

Exo'Mouv is based in France, which means its devices fall under the European Union’s regulatory framework. Since all its listed devices are classified as Class I, they are subject to EU Medical Device Regulations (MDR) or prior directives. The company registers its devices in the euDAMED database, which is the official EU registry for medical devices, ensuring compliance with EU-wide requirements.

Yes, Exo'Mouv’s devices are listed in the euDAMED database. This registry is mandatory for all medical devices placed on the EU market, ensuring transparency and traceability. Since these devices are Class I, they require registration rather than third-party certification, but listing in euDAMED confirms their compliance with EU regulatory requirements.

Exo'Mouv’s devices are classified as Class I under the EU Medical Device Regulations. This classification applies to low-risk devices like compression garments that do not require invasive procedures or sustained administration of a medicinal substance. Class I devices still must meet essential safety and performance requirements but typically undergo less stringent post-market surveillance than higher-risk classes.