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Philips provides ‘encouraging’ testing update

June 28, 2022HME News Staff

AMSTERDAM – A comprehensive testing and research program on the PE-PUR foam in certain CPAP, BiPAP and mechanical ventilator devices has shown very low prevalence of visible degradation, Philips announced in an update on June 28.  In first-generation DreamStation devices, which represent 68% of registered affected devices globally, testing found:   164 of 36,341 (0.5%) devices with self-reported no ozone use showed significant visible foam degradation.  777...

CPAP, PE-PUR, Philips Recall, Sound Abatement Foam, Testing

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