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Poly Medicure, a global leader in medical devices, has received Medical Device Regulation (MDR) certification for 54 of its products, catering to a diverse range of medical specialties, such as infusion therapy, vascular access, renal care, urology, surgery & wound care, transfusion systems, anaesthesia & respiratory care, gastroenterology, and diagnostics.
The MDR certification reaffirms that these products meet the highest safety, quality, and regulatory standards set by the European Union. This achievement marks a significant milestone for Polymed, reinforcing its commitment to providing innovative and safe medical solutions to healthcare professionals worldwide.
Rishi Baid, joint managing director of Poly Medicure said, "Our company has been the largest exporter of consumable medical devices for over a decade now. The MDR certification demonstrates that our products not only meet but exceed the most stringent safety and quality standards. We are steadfast in our commitment to these principles, which are at the core of our growth and success. With Europe already contributing half of our export revenue, this certification will further strengthen our presence and reputation in the European market. It is a testament to our focus on quality, innovation, and customer satisfaction."
An MDR certificate is a certification that a medical device complies with the European Union's Medical Device Regulation. The European Union’s MDR is a legal framework governing the production, distribution, and marketing of medical devices in the EU. It ensures medical devices meet high safety, quality, and performance standards while enhancing transparency and patient safety. The MDR is a regulation that governs the safety and performance of medical devices in the European Economic Area.
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