Verathon GlideScope Go Manual

Operations & Maintenance Manual EN
Manuel d'utilisation et de maintenance FR
Bedienungs‑ und Wartungshandbuch DE
Manual de funcionamiento y mantenimiento ES
Manuale di funzionamento e manutenzione IT
Manual de Manutenção e Operações PT
Betjenings‑ og vedligeholdelsesvejledning DA
Bedienings‑ en onderhoudshandleiding NL
Drifts‑ og vedlikeholdshåndbok NO
Drift‑ och underhållshandbok SV
0900‑4788‑06‑60

i
EN ENGLISH ..................................................................................................................... 1
Important Information................................................................................................. 1
Introduction................................................................................................................. 4
Setting Up the System ................................................................................................. 6
Using the Device........................................................................................................ 10
Cleaning & Disinfecting ............................................................................................. 13
Maintenance & Safety................................................................................................ 19
Warranty ................................................................................................................... 20
Product Specifications ............................................................................................... 20
FR FRANÇAIS ................................................................................................................ 25
Informations importantes .......................................................................................... 25
Introduction............................................................................................................... 29
Configuration du système.......................................................................................... 31
Utilisation du dispositif .............................................................................................. 35
Nettoyage et désinfection.......................................................................................... 38
Maintenance et sécurité............................................................................................. 45
Garantie .................................................................................................................... 46
Caractéristiques du produit........................................................................................ 46
DE DEUTSCH.................................................................................................................. 52
Wichtige Informationen............................................................................................. 52
Einführung................................................................................................................. 56
Einrichten des Systems............................................................................................... 58
Verwenden des Geräts .............................................................................................. 62
Reinigung und Desinfektion....................................................................................... 65
Wartung und Sicherheit............................................................................................. 73
Garantie .................................................................................................................... 74
Technische Produktdaten........................................................................................... 74
ES ESPAÑOL .................................................................................................................. 80
Información importante............................................................................................. 80
Introducción .............................................................................................................. 84
Configuración del sistema.......................................................................................... 86
Uso del dispositivo..................................................................................................... 90
Limpieza y desinfección ............................................................................................. 93
Mantenimiento y seguridad ..................................................................................... 100
Garantía .................................................................................................................. 101
Especificaciones del producto.................................................................................. 101

ii
IT ITALIANO ............................................................................................................... 108
Informazioni importanti........................................................................................... 108
Introduzione.............................................................................................................112
Configurazione del sistema.......................................................................................114
Utilizzo del dispositivo ..............................................................................................118
Pulizia e disinfezione.................................................................................................121
Manutenzione e sicurezza ....................................................................................... 128
Garanzia .................................................................................................................. 129
Specifiche di prodotto ............................................................................................. 129
PT PORTUGUÊS........................................................................................................... 135
Informações importantes......................................................................................... 135
Introdução............................................................................................................... 139
Configuração do sistema ..........................................................................................141
Utilizar o dispositivo................................................................................................. 145
Limpeza e desinfeção .............................................................................................. 148
Manutenção e segurança ........................................................................................ 155
Garantia .................................................................................................................. 156
Especificações do produto....................................................................................... 156
DA DANSK.................................................................................................................... 162
Vigtig information ................................................................................................... 162
Indledning ............................................................................................................... 166
Indstilling af systemet .............................................................................................. 168
Brug af enheden...................................................................................................... 172
Rengøring og desinfektion....................................................................................... 175
Vedligeholdelse og sikkerhed................................................................................... 182
Garanti .................................................................................................................... 183
Produktspecifikationer............................................................................................. 183
NL NEDERLANDS......................................................................................................... 188
Belangrijke informatie.............................................................................................. 188
Inleiding................................................................................................................... 192
Het systeem opstellen.............................................................................................. 194
Het apparaat gebruiken........................................................................................... 198
Reinigen en desinfecteren........................................................................................ 201
Onderhoud en veiligheid ......................................................................................... 208
Garantie .................................................................................................................. 209
Productspecificaties................................................................................................. 210

iii
NO NORSK.................................................................................................................... 216
Viktig informasjon ....................................................................................................216
Innledning ............................................................................................................... 220
Oppsett av systemet ................................................................................................ 222
Bruke enheten ......................................................................................................... 226
Rengjøring og desinfeksjon...................................................................................... 229
Vedlikehold og sikkerhet.......................................................................................... 236
Garanti .................................................................................................................... 237
Produktspesifikasjoner............................................................................................. 237
SV SVENSKA................................................................................................................ 242
Viktig information.................................................................................................... 242
Inledning ................................................................................................................. 246
Installera systemet ................................................................................................... 248
Använda enheten .................................................................................................... 252
Rengöring och desinficering .................................................................................... 255
Underhåll och säkerhet............................................................................................ 262
Garanti .................................................................................................................... 263
Produktspecifikationer............................................................................................. 263

1
EN ENGLISH
IMPORTANT INFORMATION
CONTACT INFORMATION
To obtain additional information regarding your system, please contact Verathon®
Customer Care or visit verathon.com/support.
Headquarters European Rep Manufacturer
Verathon Inc.
20001 North Creek Parkway
Bothell, WA 98011 U.S.A.
Tel: [phone] (US/Canada)
Tel: [phone]
Fax: [phone]
Verathon Medical (Europe) B.V.
Willem Fenengastraat 13
1096 BL Amsterdam
The Netherlands
Tel: [phone]
Fax : [phone]
Verathon Medical (Canada) ULC
2227 Douglas Road
Burnaby, BC V5C 5A9
Canada
Tel: [phone]
Fax: [phone]
ABOUT THIS MANUAL
Information in this manual may change at any time without notice. For the most up‑to‑date
information, see the documentation available at verathon.com/product‑documentation.
Copyright © 2018 by Verathon Inc. All rights reserved. No part of this manual may be
copied or transmitted by any method without the express written consent of Verathon Inc.
Ambient Light Reduction, DirectView, Dynamic Light Control, GlideRite, GlideScope,
GlideScope Go, the GlideScope symbol, Spectrum, Verathon, and the Verathon Torch
symbol are trademarks or registered trademarks of Verathon Inc. All other brand and
product names are trademarks or registered trademarks of their respective owners.
PRODUCT DESCRIPTION
GlideScope Go is a handheld video laryngoscope system designed to deliver clear airway
views, both directly and indirectly, facilitating rapid intubation. The reusable 3.5‑inch tilting
color monitor and rechargeable battery can be fully submerged for cleaning. Available
user settings include auto‑record, auto‑shutdown, and content display, supporting a more
customized user experience. This system integrates with the Spectrum™ product portfolio
offering fully disposable blades that can be swapped without powering down the monitor.
It also integrates with the GlideScope Video Baton 2.0, which reduces electronic waste
through the use of disposable Stats. GlideScope Go is ideal for working under rugged
conditions, for routine and difficult airways, and in a wide range of patients and clinical
settings.
STATEMENT OF INTENDED USE
The GlideScope Go System is intended for use by qualified medical professionals to obtain
a clear, unobstructed view of the airway and vocal cords for medical procedures.
STATEMENT OF PRESCRIPTION
Federal (United States) law restricts this device to sale by, or on the order of, a physician.

2
NOTICE TO ALL USERS
The system should be used only by individuals who have been trained and authorized
by a physician, or by health care providers who have been trained and authorized by the
institution providing patient care. Verathon®recommends that all users do the following:
• Read the manual before using the instrument
• Obtain instruction from a qualified individual
• Practice using the video laryngoscope on a mannequin before clinical use
• Acquire clinical training experience on patients without airway abnormalities
CAUTIONS & WARNINGS
Warnings indicate that injury, death, or other serious adverse reactions may result from
use or misuse of the device. Cautions indicate that use or misuse of the device may
cause a problem, such as a malfunction, failure, or damage to the product. Throughout
the manual, pay attention to sections labeled Important, as these contain reminders or
summaries of the following cautions as they apply to a specific component or usesituation.
Please heed the following warnings and cautions.
Medical electrical equipment requires special precautions
regarding electromagnetic compatibility (EMC) and must be installed and operated
according to the instructions in this manual. For more information, see the Electromagnetic
Compatibility section on page22.
CAUTION
Disconnect the blade or turn off the monitor in order to save a
video recording. Removing the USB flash drive before a recording has fully saved may corrupt
the video file.
CAUTION
This product may only be cleaned, disinfected, or sterilized by
using the approved low‑temperature processes recommended by Verathon.
CAUTION
Ensure the monitor's micro‑USB port is dry before connecting
a power adapter or charging cradle.
CAUTION
Ensure that you do not use any abrasive tools when cleaning
or disinfecting the monitor. The screen can be scratched, permanently damaging the device.
CAUTION
Do not submerge the charging cradle in a liquid solution.
CAUTION
The monitor must be cleaned before initial use.
WARNING
To reduce the risk of electrical shock and maintain
electromagnetic compatibility, use only the accessories and components recommended by
Verathon, including the provided, medical‑approved powersupply.
WARNING
When you are guiding the endotracheal tube to the distal tip
of the video laryngoscope, ensure that you are looking in the patient’s mouth, not at the
screen. Failure to do so may result in injury, such as to the tonsils or soft palate.
WARNING

3
Ensure that you follow the manufacturer’s instructions for
handling and disposing of cleaning, disinfection, or sterilization solutions.
WARNING
Do not reuse, reprocess, or resterilize single‑use components.
Reuse, reprocessing, or resterilization may create a risk of contamination of thedevice.
WARNING
No modification of this equipment is allowed.
WARNING
Do not attempt to open the system components. This may
cause serious injury to the operator or damage to the instrument and will void the warranty.
Contact Verathon®Customer Care for all servicing needs.
WARNING
The area surrounding the camera in the video laryngoscope
can contact the patient and can exceed 41°C (106°F) as part of normal operation. Patient
contact with this area of the blade during intubation is unlikely, as it would cause an
obstruction of the camera view. Do not maintain continuous contact with this area of the
blade for longer than 1minute; it is possible to cause thermal damage such as a burn to the
mucosal tissue.
WARNING
GlideScope blades labeled with the following part numbers
are not compatible with this system:
• 0574‑0176 (Spectrum™ LoPro S3) • 0574‑0178 (Spectrum MAC S3)
• 0574‑0177 (Spectrum LoPro S4) • 0574‑0179 (Spectrum MAC S4)
Refer to part numbers when assessing whether a blade is compatible with the system. For
more information about compatible components and accessories, see page5.
WARNING
Because the product may be contaminated with human blood
or body fluids capable of transmitting pathogens, all cleaning facilities must be in compliance
with (U.S.) OSHA Standard 29CFR1910.1030 “Bloodborne Pathogens” or an equivalent
standard. For more information, visit www.osha.gov.
WARNING
Before every use, ensure the instrument is operating correctly
and has no sign of damage. Do not use this product if the device appears damaged. Ensure
that alternative airway management methods and equipment are available.
WARNING
Ensure the monitor is clean and free of contamination before
placing it in the charging cradle.
WARNING
The charging cradle should be used only for charging the
GlideScope Go monitor.
WARNING
SYMBOLS
For a full list of caution, warning, and informational symbols used on this and other Verathon
products, please refer to the Verathon Symbol Directory at verathon.com/symbols.

4
INTRODUCTION
SYSTEM OVERVIEW
The GlideScope Go system features a small handheld monitor that can use either
GlideScope Spectrum video laryngoscopes or GlideScope GVL®Stats.
GlideScope Spectrum video laryngoscopes are durable, single‑use plastic blades that must
be disposed of after one use. Single‑use blades are identified by an S in their name, such as
LoPro S4. These blades incorporate the following technologies:
• Dynamic Light Control™—Optimizes image brightness and clarity.
• Ambient Light Reduction™—Diminishes excess reflected light to further improve
image quality.
GVL Stats are durable, transparent, single‑use laryngoscope shells that fit over a flexible,
reusable stalk called a video baton. The Stats contain no active components, so waste is
kept to a minimum. Although they are single‑use devices, they do not have an S in their
names.
Figure 1. GlideScope Go Monitor
Micro‑USB and
charging port
Connector arm
Blade/baton connector
LCD screen
Indicator LED
Power button

5
SYSTEM PARTS & ACCESSORIES
REQUIRED SYSTEM COMPONENTS
The following components are required for the system to function:
• GlideScope Go monitor
• Power adapter
INTERCHANGEABLE COMPONENTS
The system also must have one video laryngoscope connected to function. The
laryngoscope can be either a Spectrum™ blade or a video baton with a Stat, as shown in
the following list:
• Spectrum LoPro S1 (0574‑0165)
• Spectrum LoPro S2 (0574‑0166)
• Spectrum LoPro S3 (0574‑0194)
• Spectrum LoPro S4 (0574‑0195)
• Spectrum DirectView™ MAC S3 (0574‑0187)
• Spectrum DirectView MAC S4 (0574‑0188)
• GlideScope Video Baton 2.0, Large (size 3‑4, part number 0570‑0382) with one of
the following:
GVL®3 Stat (0574‑0100)
GVL®4 Stat (0574‑0101)
ADDITIONAL ACCESSORIES
The following accessories are optional and may be used with the system:
• Charging cradle
• Small carrying case
• Large carrying case
• GlideRite®Rigid Stylet (For ET tubes 6.0 mm or larger)
• GlideRite Single‑Use Stylet – Small (For ET tubes 3.0–4.0 mm)
• Micro‑to‑standard hybrid USB flash drive, for configuring settings and recording video

6
SETTING UP THE SYSTEM
PROCEDURE 1. PERFORM INITIAL INSPECTION
1. Verify that you have received the appropriate components for your system by
referring to the packing list included with the system.
2. Inspect the components for damage.
3. If any of the components are missing or damaged, notify the carrier and Verathon®
Customer Care or your local representative.
PROCEDURE 2. CHARGE THE BATTERY
To reduce the risk of electrical shock and maintain
electromagnetic compatibility, use only the accessories and components recommended by
Verathon, including the provided, medical‑approved powersupply.
WARNING
Ensure the monitor is clean and free of contamination before
placing in the charging cradle.
WARNING
For more about the battery and charging conditions, see Battery Specifications on page21.
1. Connect the power adapter to a hospital‑grade power outlet.
2. Ensure the micro‑USB port on the monitor is dry.
3. If charging directly from the power adapter, connect it to the micro‑USB port on
the monitor.
If charging with the charging cradle, connect the power adapter to the micro‑USB
port on the cradle, and then place the monitor in the cradle.
See the following table for a list of indicator LED status descriptions.
Table 1. Indicator LED Status Descriptions
LED Status Description
Solid green Battery is fully charged.
Solid orange Battery is charging with an approved or equivalent power adapter.
Solid red Battery is charging with an unapproved power adapter.*
Blinking red Error. There is a problem with the battery or charging circuit.
Off Not charging.
*Using an unapproved power adapter may not charge the battery correctly. Please replace the unapproved
power adapter with the power adapter provided with the system.

7
4. Allow the battery to charge until the indicator LED is solid green.
5. Remove the monitor from the cradle, and then press the Power button on the
monitor.
Note: Do not attach a blade or baton at this time.
6. In the upper right corner of the monitor screen, verify that the installed software
version is 1.3 or higher. If not, contact Verathon®Customer Care for a software
update.
PROCEDURE 3. CONFIGURE USER SETTINGS
The User Settings Tool is a Java‑based tool and is available on the USB flash drive.
1. Connect the USB flash drive to a USB port on a computer.
2. Navigate to the USB flash drive, and then open the User Settings Tool.
3. Configure the settings as needed, and then click Save.
4. In the Save As dialog box, navigate to the USB flash drive, and then click Save.
5. Ensure the monitor is powered off, and then insert the USB flash drive into the
micro‑USB port on the monitor.
6. On the monitor, press the Power button. The monitor powers on and the settings
automatically update. The settings file is then automatically deleted to help prevent
accidentally overwriting the date and time settings.
PROCEDURE 4. INSERT THE VIDEO BATON INTO THE STAT (OPTIONAL)
If you are using a video baton and a GVL®Stat, attach the Stat to the baton before you
connect the baton to the monitor.
1. Open the GVL Stat pouch, but do not remove the Stat from the packaging.
2. Ensure that the logo on the side of the baton and the logo on the side of the Stat
are aligned.
3. Slide the video baton into the GVL Stat until it clicks into place. Do not remove the
Stat from the pouch until you are ready to begin the intubation. This ensures that
the Stat remains as clean as possible.
Note: Ensure that you do not insert the video baton backwards.
Correct Incorrect

8
4. When you remove the GVL®Stat from the packaging, visually inspect the Stat to
ensure that all exterior surfaces are free of unintended rough areas, sharp edges,
protrusions, or cracks.
5. If desired to provide additional anti‑fog benefits, you may apply Dexide™ Fred™
Lite to the camera window on the Stat.*Use the solution according to the
manufacturer’s instructions.
PROCEDURE 5. ATTACH THE BLADE OR BATON
The blade or video baton attaches to the monitor’s connector arm. The monitor rotates on
the connector arm, allowing you to set a starting angle to begin the intubation.
It is recommended that you leave the sterile, single‑use blade in the packaging while
connecting the blade and until you are ready to perform an intubation procedure.
1. Align the arrow on the monitor with the arrow on the baton or single‑use blade,
and then insert the blade/baton connector fully into the connector port on the
blade or baton.
Alignment marks
* Compatibility has been demonstrated for up to one hour of continuous exposure on video batons and Stats.

9
PROCEDURE 6. PERFORM A FUNCTIONAL CHECK
Before you use the device for the first time, ensure the system is working properly.
1. Fully charge the monitor battery.
2. Attach the video laryngoscope to the monitor, according to the prior procedure.
3. Press the Power button. The monitor turns on.
4. Look at the screen, and verify that video is being received from the laryngoscope.
Note: The edges of the blade or Stat may be captured in the camera view. This
image acts as a frame of reference during the intubation process and ensures that
the orientation of the image is correct in the monitor.

10
USING THE DEVICE
Prior to using the device, complete the instructions in the chapter Setting Up the System.
PROCEDURE 1. PREPARE THE SYSTEM
GlideScope blades labeled with the following part numbers
are not compatible with this system:
• 0574‑0176 (Spectrum™ LoPro S3) • 0574‑0178 (Spectrum MAC S3)
• 0574‑0177 (Spectrum LoPro S4) • 0574‑0179 (Spectrum MAC S4)
Refer to part numbers when assessing whether a blade is compatible with the system. For
more information about compatible components and accessories, see page5.
WARNING
Before every use, ensure the instrument is operating correctly
and has no sign of damage. Do not use this product if the device appears damaged. Ensure
that alternative airway management methods and equipment are available.
WARNING
Table 2. Video Laryngoscope Sizes*
GlideScope Blade Part Number Recommended Patient Weight/Size
Spectrum™ LoPro S1 0574‑0165 1.5–3.8kg (3.3–8.4lbs)
Spectrum LoPro S2 0574‑0166 1.8–10kg (4–22lbs)
Spectrum LoPro S3 0574‑0194 10kg (22lbs) to medium adult
Spectrum LoPro S4 0574‑0195 40kg (88lbs) to large adult
GVL®3 Stat 0270‑0626 Medium adult
GVL®4 Stat 0270‑0628 Large adult
Spectrum DirectView™ MAC S3 0574‑0187 Medium adult
Spectrum DirectView MAC S4 0574‑0188 Large adult
1. Ensure that each GlideScope system component has been properly cleaned or
disinfected according to the guidance provided in Table 3 on page13.
2. Using the information in Table 2, in combination with a clinical assessment of the
patient and the experience and judgment of the clinician, select the GlideScope
video laryngoscope that is appropriate for the patient.
3. Attach the video laryngoscope to the monitor per Attach the Blade or Baton on
page8.
* Weight ranges are approximate; a medical professional must evaluate on a patient‑by‑patient basis.

11
PROCEDURE 2. PERFORM AN INTUBATION
The area surrounding the camera in the video laryngoscope
can contact the patient and can exceed 41°C (106°F) as part of normal operation. Patient
contact with this area of the blade during intubation is unlikely, as it would cause an
obstruction of the camera view. Do not maintain continuous contact with this area of the
blade for longer than 1minute; it is possible to cause thermal damage such as a burn to the
mucosal tissue.
WARNING
When you are guiding the endotracheal tube to the distal tip
of the video laryngoscope, ensure that you are looking in the patient’s mouth, not at the
screen. Failure to do so may result in injury, such as to the tonsils or soft palate.
WARNING
To perform an intubation, Verathon®recommends using the GlideScope 4‑Step Technique
as outlined in this procedure. Each step begins with where the user should be looking to
complete that action. Prior to beginning this procedure, verify that the monitor is receiving
an accurate image from the video laryngoscope.
1. Look in the Mouth: With the video laryngoscope in your left hand, introduce it
along the midline of the oropharynx.
2. Look at the Screen: Identify the epiglottis, and then manipulate the blade in
order to obtain the best glottic view.
3. Look in the Mouth: Carefully guide the distal tip of the tube into position towards
the tip of the laryngoscope.
4. Look at the Screen: Complete the intubation, gently rotating or angling the tube as
needed to redirectit.
PROCEDURE 3. RECORD THE INTUBATION
Disconnect the blade or turn off the monitor in order to save a
video recording. Removing the USB flash drive before a recording has fully saved may corrupt
the video file.
CAUTION
1. Start the recording by ensuring the following conditions are met:
• A blade or video baton is connected to the monitor.
• A USB flash drive is connected to the micro‑USB port on the monitor.
• The monitor is powered on.
• The record feature is turned on in the user settings.
Once these conditions are met, the recording starts automatically.
2. Stop the recording by pressing and holding the power button until the monitor
has fully powered off. The recording also stops when the video laryngoscope is
disconnected, the media capacity on the USB flash drive drops too low, or the
monitor’s remaining battery charge provides less than 1minute of power.
3. If you would like to review the recording, connect the USB flash drive to a computer,
and then view the .avi file. Files are automatically named with the system date and
time.

12
PROCEDURE 4. DISCONNECT THE BATON (VIDEO BATONS ONLY)
The GVL®Stat is a sterile, single‑use device. After each use, it is a biohazard, and it should
be removed from the video baton and disposed of in a manner consistent with local
protocols.
1. Hold the Stat in one hand.
2. To reduce the force required to remove the video baton from the Stat, use your
thumb and finger to gently press the collar of the Stat.
3. With the other hand, grasp the handle of the video baton and pull firmly.

13
CLEANING & DISINFECTING
Ensure that you do not use any abrasive tools when cleaning
or disinfecting the monitor. The screen can be scratched, permanently damaging the device.
CAUTION
This product may only be cleaned, disinfected, or sterilized by
using the approved low‑temperature processes recommended by Verathon®.
CAUTION
Because the product may be contaminated with human blood
or body fluids capable of transmitting pathogens, all cleaning facilities must be in compliance
with (U.S.) OSHA Standard 29CFR1910.1030 “Bloodborne Pathogens” or an equivalent
standard. For more information, visit www.osha.gov.
WARNING
Ensure that you follow the manufacturer’s instructions for
handling and disposing of cleaning, disinfection, or sterilization solutions.
WARNING
Do not reuse, reprocess, or resterilize single‑use components.
Reuse, reprocessing, or resterilization may create a risk of contamination of thedevice.
WARNING
The monitor must be cleaned before initial use.
WARNING
Single‑use blades arrive sterilized by ethylene oxide, and they do not require cleaning,
disinfection, or sterilization prior to use. Dispose of single‑use blades once they have been
used. Do not attempt to disinfect and reuse single‑use video laryngoscopes.
Table 3 describes the risk assessment for each system component, including the Spaulding
classification for the minimum required disinfection level. Prior to each use, ensure that
each system component has been cleaned, disinfected, or sterilized according to the
guidance provided in this table.
Table 3. System Risk Classification
Device Use Spaulding
Classification Clean Disinfect Sterile
Low High
Monitor Reusable Non‑critical X
Charging cradle*Reusable Non‑critical
Single‑use blades§Single‑use —
Video Baton 2.0|| Reusable Non‑critical X
GVL®Stats§Single‑use —
GlideRite®RigidStylet†Reusable Semi‑critical X
GlideRite Single‑Use Stylet§Single‑use —
* Clean the charging cradle when visibly soiled and on a regular basis.
†For instructions, see the GlideRite Rigid Stylet Operations and Maintenance Manual.
§Single‑use blades and stylets may not be reused. Dispose of single‑use items after use.
|| Video batons require low‑level disinfection between uses, but may be high‑level disinfected if desired.
X Checked boxes show minimum disinfection level requirement.
Shaded areas indicate that the disinfection or sterilization level is not required or not compatible with the device.
Unshaded areas show permissible levels of disinfection or sterilization based on compatibility with the device materials.

14
COMPATIBILITY & AVAILABILITY
Availability of cleaning, disinfection, and sterilization products varies by country, and
Verathon®is unable to test products in every market. Ensure that you select products
in accordance with your local laws and regulations. For information about additional
solutions that may be available, please contact Verathon Customer Care.
The following solutions have demonstrated material compatibility with the charging cradle
and monitor, and cleaning or disinfection efficacy with the monitor:
Solution Cycles
ASP®CIDEZYME®Enzymatic Detergent 1500
ASP®CIDEX®OPA Disinfectant 1500
PDI®Sani‑Cloth®AF3 Germicidal Disposable Wipe 1500
The following solutions have demonstrated material compatibility only with the monitor
through the number of use cycles shown, but have not been tested for cleaning or
disinfection efficacy. Refer to the solution manufacturers' instructions for information
about how to use them.
Solution Cycles
Clinell®Universal Wipes 1500
Metrex®CaviWipes™ 1500
Metrex®CaviWipes1™ 1500
Tristel Trio®Wipes System 1500
Wip'Anios Excel Wipes 1500
PROCEDURE 1. CLEAN THE MONITOR
Clean the monitor after each use, adhering to the instructions below. Verathon has
validated the solutions and method below for compatibility and efficacy. For information
about additional solutions that may be available, please contact Verathon Customer Care.
Table 4. Cleaning Solutions for GlideScope Go
Solution Conditions
ASP®CIDEZYME®
Enzymatic
Detergent
Up to 1500 cycles as per the following instructions:
Exposure: Prepare working solution at a concentration of 8–16 mL
per L (1–2 U.S. fluid ounces per U.S. gallon). Soak component for
1–3 minutes. Use a lint‑free cloth or cotton‑tip swab to clean the
component while still immersed, paying special attention to the
areas around the button, hinge, all surface contours, and edges.
Rinse: Rinse for 3 minutes under running water. Ensure the HDMI
connector and micro USB connector are properly rinsed.
PDI®Sani‑Cloth®
AF3 Germicidal
Disposable Wipe
Up to 1500 cycles as per the following instructions:
Exposure: Use towelette(s) to remove all visible contamination from
the component. Using fresh towelette(s), wet all surfaces and allow
to remain wet for a minimum of 3 minutes. Paying special attention
to hard‑to‑reach surface contours and edges.
Rinse: N/A. Allow the component to thoroughly air dry.