OUR HISTORY


This introduction is a tool for a better understanding of what is the production process that leads to the ingots box. Only few information can be inserted in the catalogue or in the use instructions, so many important data about process production do not reach the customer. We would like to provide a short description of processing and checks on the alloys, before of the release on the market.
Since 1998 Biesse has started a journey of certification to obtain a total control on each phase of the production process, from supplying to product release. So Biesse is certified on UNI EN ISO 13485 Medical devices. Quality management system. Requirements for regulatory purposes, under the control of Certiquality, an Italian notified institute. Furthermore, Biesse has obtained the CE marking on these products, according to European Directive 93/42, that is a compulsory requirement to distribute the alloys on the European market.