Poly Medicure has obtained Medical Device Regulation (MDR) certification for 54 of its products, ensuring compliance with the European Union’s strict safety and quality standards. The certified devices span multiple medical fields, including infusion therapy, vascular access, renal care, urology, surgery, wound care, transfusion systems, anaesthesia, respiratory care, gastroenterology, and diagnostics.

Rishi Baid, Joint Managing Director of Poly Medicure, emphasized the company's leadership in exporting consumable medical devices for over a decade. He highlighted that the MDR certification not only validates their adherence to stringent regulations but also strengthens their foothold in the European market. With Europe already contributing significantly to their export revenue, this milestone reinforces their reputation for quality, innovation, and customer satisfaction.

The MDR certification is a crucial regulatory requirement governing medical device manufacturing, distribution, and marketing within the EU. It ensures compliance with safety, quality, and performance benchmarks while enhancing transparency and patient safety across the European Economic Area.

By securing this certification, Poly Medicure further solidifies its position as a global medical device manufacturer. This achievement aligns with international regulatory frameworks and bolsters its expansion in the European market, reaffirming its commitment to delivering high-quality medical solutions worldwide.