The new Regulation MDR 2017/745 represents the European regulatory framework that establishes rules and requirements that all manufacturers and distributors of medical devices must comply with in order to market their products on the European market.

In this new legal context, Cisa Production wanted to promptly implement these changes, and in 2022 the company started the complex MDR certification process.

Today we are proud to announce the achievement of the MDR certificate for the Quality Management System which replaces Directive 93/42/EEC (MDD).

The result achieved is a confirmation of the quality and safety objectives pursued by the Management and of the commitment of all of us in obtaining the highest quality levels of our products.