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.
Category: Monitoring & Treatment
Monitoring & Treatment
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Monitoring & Treatment
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Early Alert for GE Healthcare Portrait Mobile Monitoring Software
GE HealthCare issued updated use instructions for all Portrait Mobile Monitoring Solutions operating on certain versions of Portrait Core Services software, according to an FDA early alert.
Monitoring & Treatment
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FDA Clears Masimo Pediatric Sedation Monitoring Tool
Masimo received FDA 510(k) clearance for the Patient State Index (PSi) , a new monitoring index that helps clinicians track brain activity and sedation levels in children during surgery and intensive care.
Patient Monitoring
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Drive Medical Launches Unbound IQ Brand
The new portfolio includes smart monitoring and cueing devices designed to support proactive patient care and data-driven insights.
Therapy Devices
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Early Alert for Baxter Duo-Vent Solution Sets
Baxter has recommended removal of certain Duo-Vent solution sets used for administration of fluids to the patient's vascular system.
Pulmonary Rehab
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Long COVID Patients Benefit from Cognitive Therapy
Patients with long COVID receiving individualized cognitive rehab showed significantly higher goal attainment scores at three months compared to standard care.