Medical Devices Directive information

The following information relates to the Medical Devices Directive:

• Vero EU regulatory compliance
• EU Declaration of Conformity (Vicon Vantage system)
• Vicon CE Certification
• Production quality assurance certificate
• Production quality assurance schedule
• UKCA Certificate - Production Quality Assurance
• Medical device adverse event reporting

For information on the applicable regulatory standards for Vicon Valkyrie (for both medical and non-medical sectors and industries), see Vicon Valkyrie certification and for Vicon Vero, see Vicon Vero certification.