ROSWELL, Ga., Nov. 18, 2013 /PRNewswire/ --Kimberly-Clark today announced the introduction of KimVent* MICROCUFF* Subglottic Suctioning Endotracheal Tube (ETT), the first subglottic suctioning ETT to ...

First Subglottic Suctioning ETT FDA Cleared for Saline Use(1),(2) that Provides a More Effective Suctioning to Help Prevent Cross-Contamination and Microaspiration "Clearing subglottic lines has been ...

Kimberly-Clark has launched the KimVent MICROCUFF Subglottic Suctioning Endotracheal Tube, which is the first to be FDA-cleared for saline use. The tub offers more effective subglottic suctioning and ...

The tube is FDA-approved for saline use allowing for more effective clearing of potentially harmful clogs. The device features an ergonomic subglottic suction valve and integrated rinse port, which ...

Kimberly Clark’s new Microcuff Subglottic Suctioning Endotracheal Tube is the first to be cleared by the Food and Drug Administration for saline use to more effectively clear clogs. The new Microcuff ...

FDA last week announced that Medline Industries’ recall of the Sub-G Endotracheal Tube with Subglottic Suctioning has been upgraded to the most serious type, Class I, due to the possibility that ...

Mechanical ventilation highlights the fundamental paradox of critical care: it can be both life-saving and life-threatening. Mechanical ventilation provides a bridge to recovery for patients with ...

On February 20, 2024, Medline Industries, LP initiated a nationwide recall of 6 SubG Endotracheal Tubes with Subglottic Suction and 10 kits that contain these devices. The inflation tube and other ...

The US Food and Drug Administration (FDA) has issued a Class I classification to Medline’s recall of endotracheal tubes following reports of device failures. Class I indicates the agency's most ...