Réglementation · 26 mars 2024
Certificat CE Directive 93/42/EEC Vitrobio
In our commitment to providing safe and efficient medical devices, we align with internationally recognized standards. One such standard is Directive 93/42/EEC (also known as MDD), a European Union directive that sets the framework for marketing medical devices.
Archive — article publié initialement le 2024-03-26. Les informations et documents réglementaires reflètent la situation à cette date.
Texte original conservé en anglais, comme sur l’ancienne page française.
In our commitment to providing safe and efficient medical devices, we align with internationally recognized standards. One such standard is Directive 93/42/EEC (also known as MDD), a European Union directive that sets the framework for marketing medical devices.
To demonstrate our adherence to these important standards, we are pleased to share our CE Certificate in accordance with Directive 93/42/EEC. This certificate signifies our dedication to delivering medical devices that meet rigorous quality and safety criteria.
Please click the link below to download and review our CE Certificate. This certification stands as a testament to our quality management system and our relentless commitment to safety and quality in all our medical devices.