Advice
Regulatory information
Regulatory information
myAIRVO2 is a CE marked class IIa medical device. The following Medical Device Alert for this technology has been identified:
Risk of undetected auditory alarm (2016) – updated instructions for use to check the speaker before each use because undetected auditory alarms could result in the patient becoming hypoxic. All actions outlined for this alert have been completed and the alert has been archived.