Poly Medicure Secures EU MDR Validation for Diverse Medical Devices

Poly Medicure is one of the world’s largest manufacturers of medical devices and has recently received Medical Device Regulation (MDR) validation for 54 of its products across diverse specialties such as infusion therapy, surgery & wound care, gastroenterology, renal care, urology, vascular acces, transfusion anethesia systems, respiratory care, and diagnostics.

These devices, which range from the most complex to simple infusion sets, confirm the most rigorous safety, quality, and legal criteria of the EU. This is a major milestone achievement by Polymed that reconfirms the company’s commitment to provide advanced safe medical devices to healthcare providers all over the world.

"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." Rishi Baid, joint managing director of Poly Medicure said.

An important turning point is Polymed's MDR certification, which attests to the fact that its goods satisfy the strictest safety, quality, and legal requirements established by the EU.  This accomplishment demonstrates Polymed's dedication to offering trustworthy and cutting-edge medical solutions to medical professionals around.