We are very excited to announce that our software complies with the essential requirements set by the European Union!
The CE Marking serves as a declaration from the manufacturer that their product complies with the essential requirements of the relevant European health, safety and environmental legislation laid out in the different product directives.
Once a product has been awarded the CE Marking, then it is able to move freely within the European Free Trade Association (EFTA) and the European Union (EU). In addition, our software is validated as a medical device by the Spanish Ministry of Health.
The WIVI Vision team is proud that our technology has obtained the European Conformity certificate. It’s an important step in the clinical validation of our product and a further step towards the standardization of an objective and innovative method for the assessment and treatment of visual dysfunctions.
