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Markes
 
Dear %%FirstName%%,
Respiratory medical devices are widely used in the field of medicine, but there is now growing awareness of the potential for polymeric components in the gas pathways to release harmful volatile organic compounds (VOCs).
The 2017 standard on emissions from respiratory medical devices, ISO 18562, deals with the measurement of these and other emissions, and has now been recognised by the US Food & Drug Administration. Although testing under the existing standard (ISO 10993) is still required, this development means that manufacturers can now submit their products under ISO 18562, streamlining future approvals.
Markes has released a study that describes an ISO 18562-compliant analytical setup, using pumped sampling onto sorbent tubes, followed by thermal desorption–gas chromatography–mass spectrometry (TD–GC–MS).
 
To find out more about this work, watch a short video by our Application Specialist Gareth Roberts, or download the full white paper.

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