ČSN EN ISO 18562-3 (852102)

Hodnocení biokompatibility cest dýchacího plynu ve zdravotní péči - Část 3: Zkoušky těkavých organických směsí (VOC)

ČSN EN ISO 18562-3 Hodnocení biokompatibility cest dýchacího plynu ve zdravotní péči - Část 3: Zkoušky těkavých organických směsí (VOC)
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Anotace obsahu normy

This document specifies tests for the emissions of volatile organic compounds (vocs) from 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 tests of this document are intended to quantify emissions of vocs that are added to the respirable gas stream by the materials of the gas pathway. This document establishes acceptance criteria for these tests.
This document addresses potential contamination of the gas stream arising from the gas pathways, which is then 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 gas pathways that are in direct contact with the patient. The requirements for direct contact surfaces are found in the ISO 10993 series[1].
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 devices, oxygen concentrators, nebulizers, low-pressure hose assemblies, humidifiers, heat and moisture exchangers, respiratory gas monitors, respiration monitors, masks, mouth pieces, resuscitators, breathing tubes, breathing systems filters, Y-pieces and any breathing accessories intended to be used with such 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.
This document does not address contamination already present in the gas supplied from the gas sources while medical devices are in normal use.
EXAMPLE - Contamination arriving at the medical device from gas sources such as medical gas pipeline systems (including the non-return valves in the pipeline outlets), outlets of pressure regulators connected or integral to a medical gas cylinder or room air taken into the medical device is not addressed by ISO 18562 series.
This document is intended to be read in conjunction with ISO 18562-1.
NOTE - This document has been prepared to address the relevant essential principles of safety and performance as indicated in Annex B.

Označení ČSN EN ISO 18562-3 (852102)
Katalogové číslo 510303
Cena 340 Kč340
Datum schválení 1. 9. 2020
Datum účinnosti 1. 10. 2020
Jazyk angličtina (obsahuje pouze anglický originál)
Počet stran 28 stran formátu A4
EAN kód 8596135103034
Dostupnost skladem (tisk na počkání)

Další příbuzné normy

ČSN EN ISO 18562-1 (852102)
Hodnocení biokompatibility cest dýchacího plynu ve zdravotní péči - Část 1: Hodnocení a zkoušení v rámci procesu managementu rizik

ČSN EN ISO 18562-2 (852102)
Hodnoceni biokompatibility cest dýchacího plynu ve zdravotní péči - Část 2: Zkoušky emisí pevných částic

ČSN EN ISO 18562-4 (852102)
Hodnocení biokompatibility cest dýchacího plynu ve zdravotní péči - Část 4: Zkoušky látek vyluhovatelných v kondenzátu