EN ISO 80369-1:2010

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

Publication date:   Feb 17, 2011

General information

99.60 Withdrawal effective   Nov 21, 2018

CEN/CENELEC

CEN/CLC/JTC 3 Quality management and corresponding general aspects for medical devices

European Norm

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.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Life cycle

PREVIOUSLY

WITHDRAWN
EN 15546-1:2008

NOW

WITHDRAWN
EN ISO 80369-1:2010
99.60 Withdrawal effective
Nov 21, 2018

REVISED BY

PUBLISHED
EN ISO 80369-1:2018