EU Medical Device Regulation (MDR)

Let Ansell Help with Your MDR Compliance Needs

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.

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New Resources

EU MDR Decision Tree

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.

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EU MDR Frequently Asked Questions

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.

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EU MDR Fast Facts Poster

View and download our poster with fast facts and definitions regarding the new EU MDR and what it means to operators up and down the supply chain.

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Contact Us

Contact our sales team to learn more about the new EU MDR.

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