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PRODUCTION
IV Cannula is sterilized by EO (Ethylene Oxide) Gas
The shelf life of I.V. Cannula is 5 years from the manufacturing date
Catheters are radiopaque so that they are visible using fluoroscopy. The biocompatible fluoroscopy stripes on the catheters act like markers. During fluoroscopy, the stripes absorb x-rays, making the catheter visible.
Virgin PTFE double tapered beveled tip siliconised catheter
Our I.V. Cannula with FEP/PUR/PTFE catheter range is as follows – 14G, 16G, 17G, 18G, 20G, 22G, 24G and 26G
Our 60 GSM and 100 GSM medical-grade papers keep every device sterile, protected, and audit-ready, fully compliant with ISO 11607, FDA, and CE standards. Lightweight or strong, we have the perfect paper for every product.
QUALITY
At Mais India Medical Devices Pvt. Ltd., quality, safety, and regulatory compliance are the foundation of our manufacturing processes. Our products are developed and manufactured in accordance with globally recognized quality and regulatory standards.
Our operations and Quality Management System are aligned with:
ISO 13485:2016 – International standard for quality management systems specific to the medical device industry.
European Medical Device Regulation (EU) 2017/745 – Compliance for medical devices marketed in the European Economic Area.
CE Marking – Demonstrates conformity with European health, safety, and environmental protection requirements.
Manufacturing in controlled cleanroom environments compliant with ISO 14644 for contamination control.
Through these globally recognized standards, Mais India ensures that every product meets stringent requirements for quality, patient safety, reliability, and regulatory compliance, enabling us to serve healthcare professionals and patients worldwide.