Veol Medical Technologies Pvt. Ltd.

Veol Medical Technologies manufactures surgical devices specifically designed for minimally invasive gynecological procedures. These include automated tissue retrieval systems like the Ez Catch series (Ez Catch Auto, Ez Catch YR, Ez Catch TR), a visual vasopressor injector called EzVu (EV-19), tissue morcellation containment bags named MorSafe, and a laparoscopic energy device system called Versator. These products are developed to enhance precision and safety in minimally invasive surgeries.

Veol Medical Technologies is based in India. Its devices are classified under EU Class II and Class IIa categories, which means they are subject to stricter regulatory oversight in the European Union to ensure their safety and performance. The company’s products are also listed in the EUDAMED registry, and some of its devices undergo FDA 510(k) clearance in the United States, demonstrating compliance with U.S. regulatory requirements for medical device marketing.

Veol Medical Technologies’ devices are listed in the EUDAMED registry, which is the European Union’s database for medical devices. Additionally, some of its devices are subject to FDA 510(k) clearance, meaning they are documented in the U.S. Food and Drug Administration’s premarket notification process registry. These listings reflect compliance with regulatory requirements in both the EU and the U.S.

Veol Medical Technologies’ devices are classified under EU medical device regulations as either Class II or Class IIa. This classification is determined by factors like the risk associated with the device’s use, its intended purpose, and the potential harm it may pose to patients. Class IIa devices pose a moderate risk and require additional scrutiny, while Class II devices carry a higher risk and are subject to stricter controls to ensure safety and efficacy.