Intersurgical HydroTrach BVF/HME Filter

MPIN: MP90535

Description
Store Policies

Moisture loss: 13.2mg H2O/l
Connectors: 15F
Minimum tidal volume: >60ml
Clipped suctioning port
The Intersurgical HydroTrach BVF/HME Filter is a heat and moisture exchanger, designed for use on tracheostomised patients
The HydroTrach T is an ideal HME product for prolonged use with spontaneously breathing patients
The heat and moisture exchangers filters has a clipped suctioning port accompanied with integral swivel oxygen connector and antiocclusion mechanism
Technical Specifications:
Moisture loss: 13.2mg H2O/l
Calculated Moisture Return: 26 mg H2O/I
Resistance at 30L/min: 0.2 cm H20
Resistance at 60L/min: 0.7 cm H20
Compressible volume: 19 ml
Weight: 8 g
Connectors: 15F
Minimum tidal volume: >60ml
Breathing filters are used to offer outstanding validated filtration efficiency for use in anaesthesia and intensive care. These filters are designed for the protection of the patient, hospital personnel and the equipment from potential microbial contamination.
Breathing filters and Heat and Moisture Exchangers (HME) help facilitate the normal warming, humidifying and filtering functions of the upper respiratory tract for a patient undergoing anesthesia or in intensive care. While heat and moisture exchangers regulate the inspired air by preventing the loss of moisture and heat, bacterial viral filters prevent transmission of hazardous particulate matter and microbes from the surrounding environment into the breathing system.
The use of filters is recommended to reduce the risk of crossinfection during procedures involving anesthesia if the breathing system is used for more than one patient. HME filters also reduce the need for cleaning tubing and equipment, making them more convenient for healthcare personnel when compared to the use of active humidifiers. They are bettersuited for shortterm use (less than or equal to 96 hours) and during patient transfer.
It is recommended to change the filter after each patient. The filters should be changed in every 24 hours if used on a single patient for a prolonged period.