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Adult Ventilator Articles & Analysis

5 news found

IONICON Analyzers at the Forefront of International COVID-19 Testing Research

IONICON Analyzers at the Forefront of International COVID-19 Testing Research

Grassin-Delyle et al. focused on adults undergoing invasive mechanical ventilation in the intensive care unit due to severe COVID-19 or non-COVID-19 acute respiratory distress syndrome (ARDS). ...

ByIonicon Analytik Ges.m.b.H.


Liberate Medical Reports Positive Pilot Trial Results of VentFree Respiratory Muscle Stimulator

Liberate Medical Reports Positive Pilot Trial Results of VentFree Respiratory Muscle Stimulator

Applying non-invasive electrical stimulation to the expiratory abdominal muscles may reduce abdominal muscle atrophy and markedly reduce the number of days adult patients require mechanical ventilation – a potentially important finding for weaning ventilated patients, including seriously ill COVID-19 patients, and improving patient ...

ByLiberate Medical, LLC


VentFree Respiratory Muscle Stimulator receives FDA Emergency Use Authorization for Use During COVID-19 Pandemic

VentFree Respiratory Muscle Stimulator receives FDA Emergency Use Authorization for Use During COVID-19 Pandemic

Liberate Medical today announced that it has received Federal Drug Administration (FDA) Emergency Use Authorization for its VentFree™ Respiratory Muscle Stimulator, intended to be used to reduce disuse atrophy of the abdominal wall muscles, which may reduce the number of days adult patients require mechanical ventilation, including those patients with ...

ByLiberate Medical, LLC


BioQ Pharma Receives Australian Regulatory Approval for Propofol Product - Propofusor 1%

BioQ Pharma Receives Australian Regulatory Approval for Propofol Product - Propofusor 1%

Uses of the Propofusor include the induction and maintenance of general anesthesia, sedation of mechanically ventilated adults in intensive care, and conscious sedation during diagnostic and surgical procedures. ...

ByBioQ Pharma


Liberate Medical’s VentFree Muscle Stimulator Receives Breakthrough Device Designation from the FDA to Reduce Mechanical Ventilation Duration

Liberate Medical’s VentFree Muscle Stimulator Receives Breakthrough Device Designation from the FDA to Reduce Mechanical Ventilation Duration

The proposed indication for the device is preventing breathing muscle atrophy and reducing the number of days of ventilator support in adults who require mechanical ventilation. The Breakthrough Device program is intended to expedite the process of bringing to market devices, for which no approved or cleared alternative exists, or that offer ...

ByLiberate Medical, LLC

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