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ReddyPort Inc reports US FDA's clearance for ReddyPort NIV Access Elbow in aid of patients undergoing noninvasive ventilation therapy.

M2 EQUITYBITES-March 16, 2018-ReddyPort Inc reports US FDA's clearance for ReddyPort NIV Access Elbow in aid of patients undergoing noninvasive ventilation therapy


Ventilation products company ReddyPort Inc stated on Thursday that it has been awarded the regulatory clearance from the US Food and Drug Administration (FDA) for the first multiple-use access elbow that attaches to noninvasive ventilation (NIV) masks, the ReddyPort NIV Access Elbow.

According to the company, it has a platform of unique NIV Products designed to work with the ReddyPort elbow. The ReddyPort Elbow, along with ReddyPort NIV products, provides a variety of therapies to be delivered to patients undergoing NIV therapy, without disrupting therapeutic pressure.

Additionally, the company's NIV Products for use with the ReddyPort Elbow are subject to future regulatory review.

The ReddyPort Oral Care Kit allows patients to receive routine oral care while maintaining pressure in the mask; The ReddyPort Microphone Kit amplifies a patient's voice during NIV; The ReddyPort Nebulizer is a fully enclosed vibrating mesh nebulizer designed to go through the ReddyPort Elbow; And The ReddyPort Capnography Adapter allows for accurate CO2 sampling through the mask during NIV therapy, added the company.

In conjunction with the US FDA clearance, the company will now present its ReddyPort NIV Access Elbow and NIV products at the upcoming American Association of Critical-Care Nurses Critical Care Exposition from 20-24 May 2018 in Boston.

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Publication:M2 EquityBites (EQB)
Date:Mar 16, 2018
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