Eyeol UK Limited

1.Conformity of the product device to the Medical Device Regulation and Quality Management System 2.Conformity of the Technical Documentation and EU Declaration of conformity 3.Compliance with Post-Market Surveillance (PMS) following Article 10(10) 4.Compliance with the Vigilance Reporting obligations (Article 87 to 91)

PRRC: 1.Conformity of the product device to the Medical Device Regulation and Quality Management System 2.Conformity of the Technical Documentation and EU Declaration of conformity 3.Compliance with Post-Market Surveillance (PMS) following Article 10(10) 4.Compliance with the Vigilance Reporting obligations (Article 87 to 91)