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The TRACOE smart Cuff Manager monitors and regulates the internal pressure of High Volume Low Pressure cuffs of tracheostomy tubes as well as endotracheal tubes. The pressure is continuously held between 20 cm H2O and 30 cm H2O.
Visual verification of the cuff pressure is indicated by the inflation level of the blue buffer ballon of the TRACOE smart, which should be inflated between 2/3 and 3/4. Additional checks of the cuff pressure may be performed with a cuff pressure manometer (e.g. TRACOE cpm REF 720). Is the cuff pressure too low, the TRACOE smart Cuff Manager refills the cuff quickly to its recommended pressure. Short high pressure peaks e.g. due to coughing will be tolerated by the integrated damping function which inhibits that air escapes instantly from the cuff. The solid shell of the TRACOE smart protects the highly elastic blue balloon from unwanted compression.
TRACOE smart is a latex-free, single patient product with a usage time of 29 days after opening.
REF 72X TRACOE cuff pressure monitor
1 TRACOE cuff pressure monitor
1 connecting tube (REF 702), length: 1 m
The TRACOE cuff pressure monitor is used to fill and monitor the pressure of high-volume, low pressure cuffs of tracheostomy and endotracheal tubes.
ITS OUTSTANDING FEATURES AND BENEFITS
Precise, reproducible pressure indication
Extra large, easy-to-read scale from 0 to 100 cmH2O
Widely spaced scale markings with colour coded pressure ranges
The TRACOE cuff pressure monitor comes with a connection tube with male and female Luer lock connectors on its ends (REF 702).
The subglottic secretion suction with the aim to reduce the VAP rate of patients with an expected ventilation period of more than 72 hours was classified as category IA of the recommendations by the German Commission for Hospital Hygiene and Infectious Disease Prevention (guidelines for hospital hygiene and infection prevention issued by the Robert Koch Institute, KRINKO)*. The recommendation specifies that the cuff pressure level should be set between 20 and 30 cm H2O and checked at regular intervals. The recommendation is part of category IB. When these two actions are taken in combination, they can help to reduce the incidence of pneumonia.
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