15 July 2024 | News
Positioning Noccarc at par with imported products conforming to US FDA and CE certification
Noccarc, a Pune-based medical technology company, has recently received the prestigious Bureau of Indian Standards (BIS) Certification IS 13450: Part 2: SEC 12:2023 for its Made-in-India ICU Ventilator Noccarc V730i.
This All India First License is a monumental achievement for Noccarc and marks a significant advancement for the critical medical devices industry in India. The BIS certification is a mark of excellence, highlighting the Noccarc V730i’s superior quality and performance. It demonstrates the company’s dedication to meeting the highest standards in medical technology and delivering world-class medical devices developed and manufactured in India.
This accomplishment positions Noccarc at par with imported products conforming to US FDA and CE certifications. This is especially significant given that over 80% of medical devices in India are typically imported.
The V730i has garnered endorsements from prominent medical institutions such as Apollo Hyderabad, Royal Care Coimbatore, AIIMS Bhopal, Ruby Hall Clinic, Pune, etc. These endorsements further validate the V730i’s reliability and effectiveness in critical care settings. Earlier this year, Noccarc also obtained the CDSCO Manufacturing License, which is now mandatory to manufacture ventilators in India.
The Noccarc V730i features both invasive and non-invasive ventilation modes, expansion modules such as EtCO2, Mesh nebulizer with inspiratory sync, and revolutionary remote monitoring capabilities via mobile phones, making critical care seamless and efficient.