Οι περί των Βασικών Απαιτήσεων (Ιατροτεχνολογικά Προϊόντα) (Τροποποιητικοί) Κανονισμοί του 2009.

This procedure concerns amendments to the 2009 regulations regarding the essential requirements for medical devices. These updates ensure that medical technology meets necessary safety and performance standards within the regulatory framework. Manufacturers and distributors of medical devices in Cyprus are affected by these changes, as they must comply with updated technical and safety specifications to ensure product quality and patient safety.