AVI Healthcare CE Certification Journey Featured in Medgate Today Magazine

17, June 2026

AVI Healthcare CE Certification Journey Under EU MDR 2017/745 Featured in Medgate Today Magazine

We are pleased to share that AVI Healthcare CE Certification under the European Medical Device Regulation (EU MDR 2017/745) for our VIHA dv10 ICU Ventilator has been featured in the April 2026 edition of Medgate Today Magazine.

The three-page feature highlights the significance of AVI Healthcare CE Certification under EU MDR 2017/745 and its impact on India’s medical device industry showcasing our company’s commitment to developing globally compliant medical devices while documenting the company’s regulatory journey towards achieving CE Certification under one of the world’s most demanding medical device regulatory frameworks.

The article traces the company’s evolution from a neonatal medical device manufacturer to the development of indigenous ICU ventilators during the COVID-19 pandemic. It also highlights the advanced capabilities of the VIHA dv10 ICU Ventilator and the company’s focus on engineering, regulatory compliance, and innovation.

The feature also discusses the company’s continued focus on innovation, quality management, regulatory compliance, and patient safety, while recognising another significant milestone—the company’s achievement as the first Indian medical equipment manufacturer to receive the prestigious ICMED 13485 Plus Product certification, reinforcing its dedication to maintaining the highest standards in medical device manufacturing.

Being featured in Medgate Today Magazine, one of India’s leading healthcare and medical technology publications, is a proud moment for AVI Healthcare. It reflects the growing recognition of the company’s efforts in advancing indigenous medical device manufacturing and developing healthcare technologies that meet internationally recognised quality standards.

The feature also explains how the transition from the Medical Devices Directive (MDD) to the Medical Device Regulation (EU MDR) has significantly raised regulatory expectations for medical device manufacturers. It highlights how achieving MDR certification validates not only product performance but also the robustness of engineering processes, quality management systems, risk management, and ongoing regulatory compliance.

We sincerely thank Medgate Today Magazine for featuring our journey and helping showcase the capabilities of Indian medical device manufacturers to the wider healthcare community.

Publication: Medgate Today Magazine – April 2026 Edition

Feature Pages: 44–46