The International Organization for Standardization (ISO) released the 80369-3 standard to define the design, dimensions, and functional requirements for small-bore connectors used in enteral medical devices. This global standard was developed to reduce the risk of misconnections between unrelated delivery systems, such as intravenous or respiratory devices. By ensuring incompatibility with non-enteral connectors, ISO 80369-3 helps improve patient safety and supports consistent practices across healthcare settings.
Kentec Medical’s ISOFit product line is engineered in strict compliance with the ISO 80369-3 standard. Each component in the ISOFit line is designed with the prescribed dimensions and performance characteristics to ensure compatibility within enteral systems and prevent cross-connection errors. Importantly, while we have updated the branding of this product line to better reflect our focus on safety and innovation, the core specifications remain unchanged.
Our catalog numbers, manufacturing processes, and raw materials have not been altered. ISOFit continues to represent the same trusted quality and reliability that clinicians and healthcare providers have come to expect. This branding update simply reinforces our alignment with international standards and makes it easier to identify compliant components within our enteral feeding portfolio.
Kentec remains committed to supporting healthcare professionals by delivering safe, reliable, and standards-based solutions. We actively collaborate with clinicians, caregivers, and partners across the industry to ensure our products meet the evolving needs of modern hospital environments. With ISOFit, we continue to help raise the bar for enteral feeding safety and performance.