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 ...
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 ...
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 ...
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 ...
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