Tag: respiratory equipment

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The Authority to Operate status clears the platform for use in US Department of Defense medical facilities.

ABM Respiratory Care appointed Gregory Miller as CEO effective June 1, 2024. Miller previously served as interim CEO.

Inspira Technologies received ISO 13485:2016 Standard Certification, a medical device industry standard and a step to EU regulatory approval.

The Authority to Operate status clears the platform for use in US Department of Defense medical facilities.

Dec 30, 2022

Medical technology company ABM Respiratory Care has nabbed U.S. FDA 510(k) clearance for its BiWaze Clear System.

Dec 29, 2022

The FDA is providing additional information to patients, caregivers, and healthcare providers about two recent issues in certain ventilators.

Dec 2, 2022

MediPines announced that its FDA-cleared, non-invasive pulmonary gas exchange analyzer, the MediPines AGM100, is now available in Canada.

Nov 21, 2022

Philips has experienced thousands of complaints, lawsuits, criminal investigations, and a potential DOJ settlement related to CPAP recalls.

Oct 25, 2022

Medtronic intends to pursue a separation of the company’s combined patient monitoring and respiratory Interventions businesses.

Sep 28, 2022

Philips’ recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.

Philips RS has agreed to pay nearly $1.3 million to settle allegations that it violated the False Claims Act and Anti-Kickback Statute.