This is in accordance with the U.S. FDA guidance published 22 March 2020, stating they do not object to the use of anesthesia machines for patients requiring ventilation.

IMPORTANT: This document contains off-label information. This information is only being provided for consideration during the COVID-19 pandemic. Regulatory authorities (e.g. U.S. FDA, Health Canada, TGA, EU Competent Authorities) have not cleared or approved these anesthesia devices as safe and effective for use as ICU ventilators. The use of these devices as ICU ventilators has not been verified or validated. Use of the devices in this manner is at the sole discretion and responsibility of the clinician or device owner and is done at his/her own (liability) risk.