ISO 80369-2:2024
Small-bore connectors for liquids and gases in healthcare applications - Part 2: Connectors for respiratory applications
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About This Item
ISO 80369-2:2024 is the technical reference for small-bore connectors for liquids and gases in healthcare applications, with specific focus on connectors used in respiratory applications. It is relevant to organizations that evaluate connector design, compatibility, and use in clinical equipment where connection errors can create safety risks. For engineering, procurement, and compliance teams, the document supports documented evaluation, technical review, and conformity assessment activities tied to respiratory-device interfaces and associated quality workflows.
What is ISO 80369-2:2024?
ISO 80369-2:2024 defines requirements for small-bore connectors intended for respiratory applications, helping establish a common basis for connector use in healthcare systems. It is typically used as a compliance reference when reviewing product design, validating connector interface choices, and supporting risk management for liquid and gas pathways. As the primary technical document for this subject area, it is often consulted during technical validation, laboratory evaluation, and engineering documentation reviews for respiratory-related equipment and accessories.
Applications of ISO 80369-2:2024
This document is commonly applied in the development and assessment of respiratory therapy products, medical gas delivery components, and related connectors used in healthcare environments. It may support testing workflows for interface compatibility, product evaluation during procurement, and verification activities for devices that transfer liquids or gases through small-bore connections. Manufacturers, test laboratories, and regulatory teams may use it to align technical assessments with expected connector performance and to support consistent design and documentation practices.
Why is ISO 80369-2:2024 important?
ISO 80369-2:2024 matters because connector selection and interface control can affect patient safety, operational consistency, and overall device reliability. Using a shared technical reference helps reduce the risk of misconnections, improves testing consistency, and supports clearer conformity assessment preparation. It is also useful for procurement reviews, where buyers and engineering teams need a defined basis for comparing products, confirming compatibility, and documenting compliance expectations across respiratory application workflows.
- Connector requirements for respiratory applications in healthcare liquids and gases
- Useful for design review, verification activities, and laboratory evaluation
- Supports risk management and reduction of misconnection-related safety concerns
- Relevant to procurement checks, technical validation, and compliance workflows
- Helps align engineering documentation with a recognized connector framework
- Publication Date: 2024-02-07
- Standard Status: Original
- Publisher: IEC
- Edition: 1
- This Version: ISO 80369-2:2024 (2024-02-07)
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