When you use our website, cookies are placed on your device. By clicking on "Agree", you indicate that you have read all information about our use of cookies and that you unambiguously agree to this use as set out in our cookie policy . For more information about the processing of personal data, please consult our privacy policy .
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.
Under the new MDR, the legal responsibilities of companies that sell private label gloves or act as fulfillment partners may change. Download this decision tree to see what role your company will have under the new MDR.
Download our Frequent Asked Questions document to learn more about the new MDR and what it means for different companies involved in medical glove or mask sales and distribution.