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Healthcare safety solutions

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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How to Select a Medical Glove

What are your criteria for selecting gloves? Not all gloves are made equally and there are both poor and good quality, and it is often hard to tell just by looking at them.

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Dr. Boes, an ophthalmologist from Great Falls, Montana in USA, shares a personal story on how a chemical Type IV allergy nearly ended his medical career.

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Solutions for today and tomorrow that combine advanced technologies, manufacturing, and best practice in quality assurance with a wide portfolio that meets every caregiver's needs.

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Connected to caregivers and patients through our global network of Key Opinion Leaders, clinical experts, and continuing education programs.

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Comprehensive worldwide footprint in distribution, market share, customer satisfaction, and philanthropy.

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