BS ISO 18562-1:2017 specifies:

• the general principles governing the biological evaluation within a risk management process of the gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments;
• the general categorization of gas pathways based on the nature and duration of their contact with the gas stream;
• the evaluation of existing relevant data from all sources;
• the identification of gaps in the available data set on the basis of a risk analysis;
• the identification of additional data sets necessary to analyse the biological safety of the gas pathway;
• the assessment of the biological safety of the gas pathway.

This document covers general principles regarding biocompatibility assessment of medical device materials, which make up the gas pathway, but does not cover biological hazards arising from any mechanical failure, unless the failure introduces a toxicity risk (e.g. by generating particulates). The other parts of ISO 18562 cover specific tests that address potentially hazardous substances that are added to the respirable gas stream and establish acceptance criteria for these substances.

This document addresses potential contamination of the gas stream arising from the gas pathways within the medical device, which might then be conducted to the patient.

This document applies over the expected service life of the medical device in normal use and takes into account the effects of any intended processing or reprocessing.

This document does not address biological evaluation of the surfaces of medical devices that are in direct contact with the patient. The requirements for direct contact surfaces are found in the ISO 10993 series.

Medical devices, parts or accessories containing gas pathways that are addressed by this document include, but are not limited to, ventilators, anaesthesia workstations (including gas mixers), breathing systems, oxygen conserving equipment, oxygen concentrators, nebulizers, low-pressure hose assemblies, humidifiers, heat and moisture exchangers, respiratory gas monitors, respiration monitors, masks, mouth pieces, resuscitators, breathing tubes, breathing system filters and Y-pieces as well as any breathing accessories intended to be used with such medical devices. The enclosed chamber of an incubator, including the mattress, and the inner surface of an oxygen hood are considered to be gas pathways and are also addressed by this document.


Cross References:
ISO 7396-1:2016
ISO 10993-1:2009
ISO 10993-17:2002
ISO 14971:2007
ISO 18562-2
ISO 18562-3
ISO 18562-4
ISO 10993-9
ISO 10993-13
ISO 10993-14
ISO 10993-15
ISO 13485:2016
ISO 16142-1:2016
ISO/IEC 17025
IEC 60601-1:2005
IEC 60601-1:2005/A1:2012
BS 5724-3.12


All current amendments available at time of purchase are included with the purchase of this document.