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 has been recognized with a 2022 “Best Product/Service” award in the Sustainability Category by World of Safety & Health Asia. This win recognizes the technology innovation of the Surgical SMART Pack™ and the role its innovative design plays in reducing the carbon footprint of the packaging.