The new EU Medical Device Regulation comes into effect in May 2021. That means everybody up and down the supply chain has new compliance responsibilities, a major change from the current Medical Device Directive. Failure to comply can lead to market recalls, banned goods, and even prosecution. With over 125 years of experience, Ansell has the expertise, QA systems, and product requirements in place to ensure full MDR compliance.
Ansell er af World of Safety & Health Asia blevet hædret med prisen "Best Product/Service" for 2022 inden for bæredygtighedskategorien. Denne pris er en anerkendelse af den teknologiske innovation, der findes i Surgical SMART Pack™, og den rolle, som dette nyskabende design spiller mht. til at reducere emballagens CO2-aftryk.