All products are CE marked as medical devices and comply with the rules and requirements in the legislation under the Medical Device Regulation (MDR). At Protac, our work related to MDR goes hand in hand with our high standards of quality and is an integrated part of our quality management, ultimately enhancing patient safety.

The CE mark signifies that the production complies with applicable EU regulations, and the CE mark commits Protac to documenting the quality, safety, and performance of the products, e.g., through the development of clinical evaluations.

We carefully consider the materials we use and how our production impacts the environment. Since we have high demands for the cleanliness, hygiene, and the quality of our raw material, we use, we depend on using clean, tested, and approved plastic balls in our products. For the time being plastic is the only material that can fulfill the current demands. That is why we have developed a recycling process in Denmark where we take responsibility for recycling the plastic balls from previously used products and in this way reduce the environmental impact of our production with regards to plastic consumption and CO2 emission.

With this initiative, we want to make it easy for our customers to return used Protac products to us and make it possible for ourselves to reuse our own plastic of a well-known and approved quality in the production of new balls.
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