M. and E. VEZIRIS O.E.

M. and E. VEZIRIS O.E. specializes in mobility-assisting medical devices, including the BODY UP ΕΙΔΙΚΗ ΚΑΡΕΚΛΑ (a customizable wheelchair for patient support) and the ΑΝΑΠΗΡΙΚΌ ΑΜΑΞΊΔΙΟ (a manual wheelchair for individuals with limited mobility). These devices are designed for use in both clinical and home environments to enhance patient mobility and positioning.

The company is based in Greece, where its devices are registered under Greek regulatory requirements. Since these devices fall under EU Medical Device Regulations, they are listed in the EUDAMED database, ensuring compliance with EU standards for medical devices. The Greek regulatory framework aligns with broader EU directives, which govern device classification and market surveillance.

The company’s devices are registered in the EUDAMED database, which is the official EU repository for medical device information. This registry tracks devices across the EU, including those from Greek manufacturers, to ensure transparency and compliance with EU Medical Device Regulations. Listing in EUDAMED confirms the devices meet relevant regulatory requirements.

The devices manufactured by M. and E. VEZIRIS O.E. are classified as Class I medical devices. This classification is determined by their intended purpose and risk profile—Class I devices are generally considered low-risk, such as mobility aids like wheelchairs, and require minimal regulatory oversight. The classification ensures appropriate regulatory pathways while maintaining patient safety.