Biocompatibility Testing of Respiratory Medical Devices to ISO 18562

New versions of the ISO 18562 Biocompatibility standards have been published to provide updated guidance for the evaluation of respiratory medical devices.

THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.

Watch now: Biocompatibility testing of respiratory medical devices to ISO 18562

A webinar on new versions of the ISO 18562 biocompatibility standards provides updated guidance for the evaluation of respiratory medical devices.

Webinar date

May 28, 2024

Speakers

Scott Laughlin, program manager, GREENGUARD Certification Program, Product Emissions, UL Solutions
Florian Rauh, head of analytical chemistry department, Consumer, Medical and Information Technologies, UL Solutions
Eric Rosenblum, diplomate of the American Board of Toxicology

The webinar session provides an overview of the latest updates to the ISO 18562 series of standards.

These standards outline the general principles for the biocompatibility evaluation of breathing gas pathways of medical devices used in respiratory care or to supply anesthesia or other substances through the respiratory tract.

Revised versions of the four standards in the ISO 18562 series are being published to provide updated guidance based on lessons learned since they were first published in 2017.

The webinar session provides an overview of the latest updates to the ISO 18562: 2024 series with the aim of helping producers of breathing gas pathways identify what they are compared to the 2017 version.

Watch our webinar to gain a better understanding of how these updates may impact your business.