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Intersurgical i-view Gebrauchsanweisung Seite 5

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Pre-use checks
• Inspect the packaging and ensure it is not damaged prior to opening.
• Inspect the device carefully and discard if the device looks abnormal or deformed.
• Turn on the device by depressing the on/off switch (fig 1) and check there is a visible light at the distal end
of the blade and that the Intersurgical logo appears on the screen for a few seconds. Also ensure that the
camera is working correctly. Turn off the device by depressing the on/off button. The device is now fully
operational. Discard the device if it cannot be successfully switched on and off.
• In order to reduce the potential for battery depletion, i-view will automatically switch itself off after 20
minutes. If required, the device can be switched on again by pressing the on/off button.
Using the i-view
• Turn on the device by pressing the on/off button (fig 1).
• The distal tip of the blade of the device should be inserted into the patient's mouth under direct
vision (fig 2) and the blade gently advanced down the tongue until the epiglottis has been
identified (fig 3). The tip of the blade should then be advanced into the vallecula (fig 4).
• With minimal force, indirectly lift the epiglottis with the i-view until the glottis comes into view. This can be
achieved using a direct or indirect view (fig 5). If deemed necessary, bimanual laryngoscopy and/or head
elevation can be used to improve the view.
• Once the glottis has been identified, an appropriately sized tracheal tube can be passed through the vocal
cords to the required depth (fig 6) and the i-view gently removed (fig 7).
• Confirmation of correct placement of the tracheal tube should be assessed by the use of wave form
capnography and other methods in accordance with applicable guidelines.
• i-view should then be switched off by depressing the on/off switch (fig 8).
Storage Conditions
Recommended storage at room temperature over the indicated product shelf life. Store in a dry place out
of direct sunlight.
Disposal
Following use, the product must be disposed of in line with the local healthcare, hygiene and waste disposal
protocols and regulations.
Specification
Size
Weight
Minimum Interdental Gap
Electrical Rating:
Applicable Standards
EN 60601-1:2006 + A11:2011
EN 60601-1-6:2010
EN 62366:2008
EN 60601-1-12:2014
200 mm x 162 mm x 70 mm
0.138 kg
16 mm
4.5V DC 150mA
5

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