FDA Clears Getinge Edi Catheter
The FDA granted 510(k) clearance to Getinge's 6Fr/48 cm Edi catheter designed for premature infants weighing between 500 and 1,000 grams.
The FDA granted 510(k) clearance to Getinge's 6Fr/48 cm Edi catheter designed for premature infants weighing between 500 and 1,000 grams.
The FDA granted 510(k) clearance to Getinge’s 6Fr/48 cm Edi catheter designed for premature infants weighing between 500 and 1,000 grams.
Read MoreNeonatal pulmonary disorders may require additional respiratory support beyond supplemental oxygen, such as nasal CPAP, HFNC, nasal BiPAP, NIPPV, nHFOV, or even NIV-NAVA.
Read MoreGetinge launched its new Servo-c mechanical ventilator targeting selected markets, offering lung-protective therapeutic tools to treat both pediatric and adult patients, according to a company news release.
Read MoreWith this launch, Neurally Adjusted Ventilatory Assist is now available for both neonatal and adult patients.
Read MoreMaquet Critical Care has launched its Neurally Adjusted Ventilatory Assist (NAVA) for noninvasive ventilation in neonatal patients.
Read MoreRT spoke with Doug Smith, vice president critical care, Maquet, about what it takes to win the Frost & Sullivan Market Leadership Award and how the company plans to continue demonstrating market strength.
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