ISO 80369-1:2010

Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements ISO 80369-1:2010

Publication date:   Dec 8, 2010

95.99 Withdrawal of Standard   Nov 5, 2018

General information

95.99 Withdrawal of Standard   Nov 5, 2018

ISO

ISO/TC 210 Quality management and corresponding general aspects for medical devices

International Standard

11.040.10   Anaesthetic, respiratory and reanimation equipment | 11.040.20   Transfusion, infusion and injection equipment

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Scope

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.

Life cycle

NOW

WITHDRAWN
ISO 80369-1:2010
95.99 Withdrawal of Standard
Nov 5, 2018

REVISED BY

PUBLISHED
ISO 80369-1:2018