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Getinge Flow-i User Manual

Getinge Flow-i
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Page 3
MX-7711-02
WWW.GETINGE.COM
- Please be aware that nebulization of drugs is not approved with this anesthesia device.
Using aerosol therapy might affect the device negatively causing malfunctinon.
- The anesthesia device is not validated or intended for use with active humidication. Should
this nevertheless be used the HME filter at the y-piece cannot be connected to the system,
as the humidification created will be filtered by the HME filter and will thus not reach the
patient. This will most likely also result in excessive condensate in the anesthesia device. If
active humidification is used the system shall run with high fresh gas flows and be
equipped with filters on both the inspiratory and expiratory limbs and close monitoring of
the ventilatory and patient parameters is mandatory. Dual heated breathing circuits should
not be used.
- If inhalation anesthestic agents are used as sedation the user must be aware of that the
surplus of the agents could be transported out into the environment. It is therefore
important to connect an Anesthesia Gas Scavenging System (AGSS) to the system.
- Reprocessing of applicable parts of the the anesthesia device shall be performed
according to the information in the Cleaning and Maintenance Manual, ie between each
patient after treating a known carrier of pulmonary contagious agents.
- Please ensure that the system has the latest avaliable software installed.
MCV00103387 REVA

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Getinge Flow-i Specifications

General IconGeneral
BrandGetinge
ModelFlow-i
CategoryMedical Equipment
LanguageEnglish

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