EN ISO 80369-1:2010

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Materials used for SMALL-BORE CONNECTORS
5 Requirements for SMALL-BORE CONNECTORS for specific
  APPLICATIONS
6 Additional SMALL-BORE CONNECTOR APPLICATIONS
7 PROCEDURE to assess a proposed new design of SMALL-BORE
  CONNECTOR for inclusion in this series of standards
Annex A (informative) - Rationale
Annex B (normative) - Mechanical tests for verifying
        NON-INTERCONNECTABLE characteristics
Annex C (informative) - APPLICATIONS of SMALL-BORE CONNECTORS
Annex D (informative) - Reference to the Essential Principles
Bibliography
Terminology - Alphabetized index of defined terms
Annex ZA (informative) - Relationship between this European
         Standard and the Essential Requirements of EU
         Directive 93/42/EEC

ISO 80369-1:2010 specifies general requirements for small-bore connectors, which convey liquids or gases in healthcare applications. These small-bore connectors are used in medical devices or accessories intended for use with a patient. ISO 80369-1:2010 also specifies the healthcare fields in which these small-bore connectors are intended to be used.These healthcare fields of use include, but are not limited to, applications for:breathing systems and driving gases, enteral and gastric, urethral and urinary, limb cuff inflation, neuraxial devices, and intravascular or hypodermic. Small-bore connectors as specified in ISO 80369-1:2010 are non-interconnectable with:the cones and sockets of ISO 5356-1:2004 and ISO 5356-2:2006; the temperature sensor connector and mating ports specified in Annex DD of ISO 8185:2007; and the nipples of EN 13544-2:2002. ISO 80369-1:2010 provides the methodology to assess non-interconnectable characteristics of small-bore connectors based on their inherent design and dimensions in order to reduce the risk of misconnections between medical devices or between accessories for different applications and to reduce the risk of misconnections between medical devices with 6 % Luer connectors, and all other non-Luer (6 %) connectors that will be developed under future parts of this series of standards.It does not specify requirements for the medical devices or accessories that use these small-bore connectors. Such requirements are given in particular International Standards for specific medical devices or accessories.