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 ...

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 ...

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 ...

He also serves as the Research Director of the Critical Care Program at Queen’s and KGH. The study will compare the CeraShield ETT’s efficacy to that of an uncoated endotracheal tube with subglottic ...

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 ...

This double blind, stratified, randomized placebo control trial was conducted between November 2007 and April 2009. Eligible participants were patients aged 3 months to 15 yrs who required orotracheal ...

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 ...

Medline told customers of 89 lots of endotracheal tubes to destroy inventory after receiving reports of the inflation tube tearing and detaching, the FDA said June 11. The medical devicemaker’s Sub-G ...

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 ...