GlobalData on MSN1d
FDA tags Sentec/Percussionaire’s breathing circuit recall as Class IFailed to fetch dynamically imported module: https://finance.yahoo.com/assets/_app/immutable/nodes/105.DOJoPAWP.js ...
This device delivers a steady concentration of nitric oxide (NO), a vasodilator, into the inspiratory limb of the patient’s ...
* Beyond Air's LungFit PH is approved for commercial use in the United States of America, European Union, Australia and New Zealand. Beyond Air's other LungFit systems are not approved for commercial ...
Zaynich could play a key role in treating patients suffering from complicated urinary tract infections caused by ...
When the first outbreak happened in Pune, all heads turned and started to panic. What was this new infectious intruder? How ...
India has exported fresh produce such as baby corn and pomegranates to 17 new markets, such as Brazil, Georgia, Uganda, and ...
As for discharges, hospitals have released 25 patients so far. But on ventilator support are 18 patients while 45 others are in ICUs. An official from the state's Rapid Response Team, which has ...
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
The number of suspected cases of Guillain-Barre Syndrome (GBS) has reached 140 with four suspected deaths due to the disease in Maharashtra. Of the 140 suspected cases, 98 are diagnosed as ...
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