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FDA tags Sentec/Percussionaire’s breathing circuit recall as Class I
The US Food and Drug Administration (FDA) has tagged a recall of breathing circuits manufactured by Sentec/Percussionaire as ...
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Australian TGA authorises marketing of Beyond Air’s LungFit PH system
The Australian Therapeutic Goods Administration (TGA) has granted authorisation to market Beyond Air’s LungFit PH as a Class IIb medical device. This device delivers a steady concentration of nitric ...
standardmedia.co.ke3y
Not every patient needs a ventilator, life support machine
But medics have since found out that not every patient is supposed to be put under a ventilator or a life support machine. Siika recalls: “In the beginning, we were quick to intubate ...
Business Insider22d
Beyond Air® Announces LungFit® PH Receives Market Authorization in Australia
generated by the device into the inspiratory limb of the patient breathing circuit of a ventilator in a way that provides a constant concentration of nitric oxide, as set by the user, to the patient ...