Verathon 0900-4200-xx-60 GLIDESCOPE SYSTEM AVL SINGLE‐USE Operations & Maintenance Manual

GLIDESCOPE SYSTEM

AVL SINGLE‑USE

Operations & Maintenance Manual

0900‑4200 REV‑11

GLIDESCOPE SYSTEM

AVL SINGLE‑USE

Operations & Maintenance Manual

Effective: January 8, 2021

Caution: Federal (United States) law restricts this

device to sale by or on the order of a physician.

For customers with GlideScope systems using the GlideScope Video Monitor (version 0570‑0338).

CONTACT INFORMATION

To obtain additional information regarding your GlideScope system,

please contact Verathon Customer Careor visit verathon.com/global‑support.

Verathon Inc.

20001 North Creek Parkway

Bothell, WA 98011 U.S.A.

Tel: [phone] (US and Canada only)

Tel: [phone]

Fax: [phone]

verathon.com

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]

Verathon Medical (Australia) Pty Limited

Unit 9, 39 Herbert Street

St Leonards NSW 2065

Australia

Within Australia: 1800 613 603 Tel / 1800 657 970 Fax

International: [phone] Tel / [phone] Fax

Copyright © 2021 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.

GlideRite, GlideScope, the GlideScope symbol, GVL, Reveal, Verathon, and the Verathon Torch symbol are trademarks of Verathon Inc.
All other brand and product names are trademarks or registered trademarks of their respective owners.

Not all Verathon Inc. products shown or described in this manual are available for commercial sale in all countries.

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.

TABLE OF CONTENTS

IMPORTANT INFORMATION .................................................................................................................................1

Product Information ............................................................................................................................................1

Statement of Intended Use ..................................................................................................................................1

Essential Performance .........................................................................................................................................1

Environments of Intended Use.............................................................................................................................1

Statement of Prescription ....................................................................................................................................1

Notice to All Users ..............................................................................................................................................1

Warnings & Cautions ..........................................................................................................................................2

Product Description ............................................................................................................................................6

INTRODUCTION ....................................................................................................................................................8

System Parts & Accessories .................................................................................................................................8

Language Settings ............................................................................................................................................ 11

Video Laryngoscope Components ..................................................................................................................... 12

Buttons, Icons, & Connections ......................................................................................................................... 13

SETTING UP ......................................................................................................................................................... 16

Procedure 1. Perform Initial Inspection ..................................................................................................... 16

Procedure 2. Mount the GlideScope Video Monitor (Optional) .................................................................. 17

Procedure 3. Attach the Video Baton Cradle (Optional) .............................................................................20

Procedure 4. Charge the Monitor Battery ................................................................................................. 21

Procedure 5. Connect the Video Cable or Smart Cable to the Monitor ...................................................... 22

Procedure 6. Connect the Smart Cable to the Video Baton (VideoBaton2.0Only) ....................................23

Procedure 7. Connect to an External Monitor (Optional) ........................................................................... 24

Procedure 8. Configure User Settings ....................................................................................................... 25

Procedure 9. Perform a Functional Check .................................................................................................26

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USING THE DEVICE .............................................................................................................................................28

Procedure 1. Connect the Video Cable to the Monitor ..............................................................................29

Procedure 2. Insert the Video Baton into the Stat......................................................................................30

Procedure 3. Prepare the GlideScope System ............................................................................................ 30

Procedure 4. Intubate Using a Video Baton and Stat ................................................................................. 31

Procedure 5. Use the Record & Snapshot Features (Optional) ....................................................................32

Procedure 6. Use the Playback Feature (Optional) .....................................................................................34

Tips for Using the GlideScope AVL System .........................................................................................................35

Tips for Working with Endotracheal Tubes ......................................................................................................... 35

REPROCESSING .................................................................................................................................................... 36

MAINTENANCE & SAFETY .................................................................................................................................. 37

Periodic Inspections ..........................................................................................................................................37

GlideScope Video Monitor Battery ....................................................................................................................37

System Software ............................................................................................................................................... 37

Device Repair ....................................................................................................................................................38

Device Disposal ................................................................................................................................................. 38

WARRANTY.........................................................................................................................................................39

PRODUCT SPECIFICATIONS ................................................................................................................................. 41

Component Specifications ................................................................................................................................41

Battery Specifications ........................................................................................................................................49

Electromagnetic Compatibility ...........................................................................................................................50

Accessory Conformance to Standards ................................................................................................................52

GLOSSARY ...........................................................................................................................................................53

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IMPORTANT INFORMATION

PRODUCT INFORMATION

The GlideScope AVL Single‑Use video laryngoscope system is designed for “1st Pass Success.” It provides
a consistently clear view of a patient’s airway, enabling quick intubations. The AVL design is based on the
GlideScope GVL, which is clinically proven to achieve a Cormack‑Lehane Grade I or II view 99 percent of the
time.

STATEMENT OF INTENDED USE

The GlideScope AVL system is intended for use by qualified professionals to obtain a clear, unobstructed view
of the airway and vocal cords for medical procedures.

ESSENTIAL PERFORMANCE

Essential performance is the system performance necessary to achieve freedom from unacceptable risk. The
essential performance of the GlideScope AVL system is to provide a clear view of the vocal cords.

ENVIRONMENTS OF INTENDED USE

The GlideScope AVL system is intended to be used in professional healthcare environments such as hospitals.

STATEMENT OF PRESCRIPTION

Caution: Federal (United States) law restricts this device to sale by or on the order of a physician.

This system should be used only by individuals who have been trained and authorized by a physician or used
by healthcare providers who have been trained and authorized by the institution providing patientcare.

NOTICE TO ALL USERS

Verathon recommends that all users read this manual before using the system. Failure to do so may result in
injury to the patient, may compromise the performance of the system, and may void the system warranty.
Verathon recommends that new GlideScope users:

• Obtain instruction from a qualified individual

• Practice using the system on a mannequin before clinical use

• Acquire clinical experience on patients without airway abnormalities

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WARNINGS & CAUTIONS

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.

WARNINGS

WARNING

Several areas of the Stat that contact the patient can exceed 41°C (106°F) as part of normal
operation:

•The first area is the light‑emitting area surrounding the camera. When used as indicated,
continuous contact with this area is unlikely because, if tissue were to contact this area, the view
would be lost and devices would need to be adjusted to regain the airway view.

•The second area is the area surrounding the camera, out of view of the camera. Continuous
contact with this area is unlikely because the product is typically not held stationary for an
extended period of time exceeding 1minute.

If continuous contact is maintained 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

Before every use, ensure that the instrument is operating correctly and has no sign of damage.
Do not use this product if the device appears damaged. Refer servicing to qualified personnel.

Always ensure that alternative airway management methods and equipment are readily
available.

Report any suspected defects to Verathon Customer Care. For contact information, visit
verathon.com/global‑support.

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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.

WARNING

This product may only be cleaned, disinfected, or sterilized by using the approved processes
provided in the GlideScope and GlideRite Products Reprocessing Manual (part number 0900‑

5032). Cleaning, disinfection, and sterilization methods listed are recommended by Verathon
based on efficacy or compatibility with component materials.

WARNING

To maintain electrical safety, use only the provided power supply. Connect the power cord and
power adapter to a properly grounded plug, and ensure that the disconnect is easily accessible.
Use only the accessories and peripherals recommended by Verathon.

WARNING

To reduce the risk of electrical shock, use only the accessories and peripherals recommended by
Verathon.

WARNING

Electric shock hazard. Do not attempt to open the system components. This may cause serious
injury to the operator or damage to the instrument and voids the warranty. Contact Verathon
Customer Care for all servicing needs.

WARNING

No modification of this equipment is allowed.

WARNING

The external monitor must be safety‑approved medical equipment.

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WARNING

Use only a passive‑type USB flash drive. Do not use USB drives powered by another
externalsource.

WARNING

Electric shock hazard. Do not immerse the power adapter in water. When cleaning the power
adapter, use a cloth dampened with isopropyl alcohol on the outside of the enclosure.

WARNING

Verathon has conducted no analysis to establish the compatibility of the system with
environments where magnetic resonance imaging (MRI) equipment is installed. Because of this,
the owner of the system must exclude it from any magnetic resonance (MR) environment.

WARNING

Do not use the power adapter in the presence of flammable anesthetics.

WARNING

Do not reuse, reprocess, or resterilize single‑use components. Reuse, reprocessing, or
resterilization may create a risk of contamination of thedevice.

WARNING

WARNING

Use of accessories and cables other than those specified or provided by Verathon may cause this

Use of accessories and cables other than those specified or provided by Verathon may cause this
system to experience electromagnetic malfunctions, including increased emissions or decreased

system to experience electromagnetic malfunctions, including increased emissions or decreased
immunity. This may cause improper operation, procedure delays, or both.

immunity. This may cause improper operation, procedure delays, or both.

WARNING

Portable radio frequency communications equipment (including peripherals such as antenna
cables and external antennas) may not be used within 30 cm (12 inches) of any part of the
GlideScope system, including cables that Verathon specifies or provides for use with the system.
If this distance is not maintained, performance of the system may be degraded and image
display may be compromised.

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CAUTIONS

CAUTION

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.

Avoid using the GlideScope system adjacent to or stacked with other equipment. If adjacent or
stacked use is necessary, observe the system to verify normal operation in the configuration in
which it will be used.

This device can radiate radio frequency energy and is highly unlikely to cause harmful
interference with other devices in the vicinity. There is no guarantee that interference will
not occur in a particular installation. Evidence of interference may include degradation of
performance in this device or other devices when operated simultaneously. If this occurs, try to
correct the interference by using the following measures:

•Turn devices on and off in the vicinity to determine the source of interference

•Reorient or relocate this device or other devices

•Increase the separation between devices

•Connect the device to an outlet on a circuit different than the other device(s)

•Eliminate or reduce EMI with technical solutions (such as shielding)

•Purchase medical devices that comply with IEC60601‑1‑2 EMC standards

Be aware that portable and mobile radio frequency communications equipment (cellular phones,
etc.) may affect medical electrical equipment; take appropriate precautions during operation.

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PRODUCT DESCRIPTION

The GlideScope AVL system is an ideal tool for physicians and other healthcare professionals who need to
effectively manage routine to difficult airways. It is useful for the intubation of normal airways, anterior
airways, neonatal patients, obese patients, and patients with limited neck extension. Additionally, it is
useful for teaching purposes, verification of endotracheal tube (ETT) placement, nasal intubation, and
ETT exchange. The AVL is easy to learn, use, and teach. It is ideal for acute care settings and emergency
environments. It also integrates into standard ED, OR, ICU, and NICU applications.

The system combines a high‑resolution, full‑color digital camera with an integrated LED light source and
Reveal anti‑fog feature. The video batons connect directly to a full‑color, digital video monitor for real‑time
viewing.

The system is recommended for use with an endotracheal tube stylet such as the GlideRite Rigid Stylet or the
GlideRite Single‑Use Stylet, which complements the blade angle.

GLIDESCOPE VIDEO MONITOR

The monitor can record video and photos directly to a USB flash drive for archiving and further review.
The monitor has a DVI video output through an HDMI connector. It is recommended that you use the
HDMI‑to‑DVI cable provided by Verathon to connect to an external monitor that is approved for medical use.
You can operate the monitor by connecting it to the medical‑grade power supply provided by Verathon or by
using the internal, rechargeable lithium‑ion battery.

Verathon occasionally makes software updates available for the GlideScope video monitor. This manual
documents the most current version of the GlideScope Video Monitor software. If your monitor does not
function as described in this manual, or to determine if your software should be updated, contact Verathon
Customer Care.

Figure 1. GlideScope Video Monitor

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SINGLE‑USE SYSTEM

The AVL single‑use system can be used with a choice of three video batons and multiple GVL Stats.
Single‑use GVL Stats are offered in a comprehensive range of sizes, allowing clinicians to meet the particular
requirements of patients of various sizes.

The system may include the following components:

• GlideScope Video Monitor

• AVL Video Baton 1–2
○ GVL 0 Stat
○ GVL 1 Stat
○ GVL 2 Stat
○ GVL 2.5 Stat

• Video Baton 2.0 Large (3–4) or AVL Video Baton 3–4
○ GVL 3 Stat
○ GVL 4 Stat

• GlideRite Single‑Use Stylet (Small; recommended for use with the AVL Video Baton 1–2)

• GlideRite Single‑Use Stylet (Large) or GlideRite Rigid Stylet (recommended for use with the Video

Baton 2.0 Large (3–4) or AVL Video Baton 3–4)

Note: Video Batons 2.0 require GlideScope Video Monitor software version 3.9 or later. For more
information, refer to System Software on page37.

Figure 2. GlideScope AVL Single‑Use System

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INTRODUCTION

SYSTEM PARTS & ACCESSORIES

The system consists of the following components.

Table 1. System Components

PARTS & ACCESSORIES

Required Components

GlideScope Video Monitor Video batons

GVL Stat sizes 0, 1, 2, 2.5, 3, and 4 (single‑use)

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PARTS & ACCESSORIES

Smart Cable

(for Video Baton 2.0)

Note: Cable shortened for

illustrationpurposes.

Power cable

Video monitor 12V DC

poweradapter

In‑service USB flash drive

Note: Contains instructions for use.

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PARTS & ACCESSORIES

Optional Components

Premium cart

Mobile stand

Universal accessory basket

Note: For use with AVL portablestand

Media storage USB flash drive

Cradle for video baton IV pole mounting kit HDMI‑to‑DVI cable

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PARTS & ACCESSORIES

GlideRite DLT Stylet

Note: For ET tubes 6.0mm orlarger

GlideRite Single‑Use Stylet (Small)

Note: For ET tubes 3.0–4.0mm

GlideRite Rigid Stylet

Note: For ET tubes 6.0mm orlarger

GlideRite Single‑Use Stylet (Large)

Note: For ET tubes 6.0mm orlarger

LANGUAGE SETTINGS

The GlideScope Video Monitor software is available in a variety of languages. To change the language
used on your system, you must install a new software version via a USB flash drive. For more
information, contact Verathon Customer Care or your local representative. For contact information, visit

verathon.com/global‑support.

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VIDEO LARYNGOSCOPE COMPONENTS

The following diagram shows the individual parts of an AVL video laryngoscope (a reusable video baton with
a single‑use Stat).

Figure 3. AVL Video Laryngoscope Components

Camera and light

Single‑use Stat

Smart Cable

Video baton

Video cable
(permanently
attached)

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BUTTONS, ICONS, & CONNECTIONS

The main component of the system is the digital, full‑color monitor. The front of the monitor includes the
screen and the buttons you use to operate the system.

The back panel of the monitor includes the sockets and ports for connecting the power cord, the video
cable, an HDMI‑to‑DVI cable for external video display, and a USB flash drive. When a socket or port is
not in use, it is recommended that the rubber cap is inserted into the opening. This protects the exposed
connectors from dust and other contamination. The back of the video monitor also features a mounting plate
fitting that allows you to attach the monitor to a mobile stand or IV pole.

Figure 4. GlideScope Video Monitor Keypad

Record button External Video button

Power button Snapshot button

Tutorial button

Table 2. Keypad Buttons

BUTTON FUNCTION

Power: Press and release to turn on the monitor. Press and hold to turn it off.

Note: If the monitor freezes at any time during use, press and hold the Power button for
10seconds to reset the system.

Record: Press to start and stop recording directly to a USB flash drive that has been inserted
in the USB port. When you are recording, the red LED indicator to the right of the button will
be lit, and the Recording icon will be shown on the screen.

Note: To record video, a USB flash drive must be inserted into the monitor USB port.

Snapshot: Press this button to save a snapshot of the live display to the USB flash drive. You
may take a snapshot while video recording or independent of recording.

Note: To take a snapshot, a USB flash drive must be inserted into the monitor USB port.

External Video: Press to display video on an external monitor. The yellow LED to the right
of the button will light up to indicate that the feature has been activated. Press the button
again to deactivate the external video.

Battery indicator

Note: An HDMI‑to‑DVI cable is required in order to display video on an external monitor.

Tutorial: If a USB flash drive is not inserted into the monitor, press and hold to access the
video tutorial. If a USB flash drive is inserted into the monitor, press and hold to access the
Playbackmenu.

Note: The Playback menu is only accessible if the GlideScope Video Monitor is operating
software version3.4 or higher and if a USB flash drive is inserted in the monitor.

Battery Indicator: LED is:

Green: Unit fully charged
Red: Unit charging
Flashing Red: Indicates a problem with the battery. Charge for 6hours, and if still

flashing, contact Verathon Customer Care.

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Table 3. On‑Screen Icons

ICON FUNCTION

Battery Status: The remaining battery power is indicated by the Battery Status

icon and the percentage above the icon. If the icon is red, the battery should be
charged as soon as possible. (See Charge the Monitor Battery.) While the battery
is being charged, a lightning bolt will be displayed alongside the Battery Status
icon.

Progress Confirmation: While the user is pressing a button, the operation is
loading. If the button is released before the loading process is completed, the
operation is canceled.

Power‑Down Countdown: The unit is about to turn off. If this is due to the
Auto Power Off feature that saves battery life, pressing any button stops the
power‑down sequence.

Note: The Auto Power Off feature can be adjusted or disabled on the User
Settings screen. For more info, see Configure User Settings on page25.

USB Flash Drive: A USB flash drive is detected.

While recording, a number next to the icon indicates approximately what
percentage of the USB flash drive has been used. When the USB flash drive is full,
recording stops.

Incompatible USB Drive: The USB flash drive that is plugged into the monitor
is not suitable for recording videos. (This normally occurs when using an older,
inexpensive USB flash drive that is not capable of the speed necessary to save
video in real time.)

USB Flash Drive Not Found: A USB drive needs to be inserted into the USB port.

Attach Video Cable: The video baton or video laryngoscope is not attached to

themonitor.

Recording: The system is recording video to the USB flash drive.

Note: Do not remove the USB flash drive while recording is in progress, or the
recording will be lost.

Saving Snapshot: The system is saving a snapshot to USB flash drive.

Note: Do not remove the USB flash drive while saving a snapshot, or the snapshot
will be lost.

Saving File: The system is saving a recorded file to the USB flash drive.

Note: Do not remove the USB flash drive while this icon is displayed, or the
recording will be lost.

External Monitor: The HDMI‑to‑DVI connection for external video is enabled.
Videomay now be displayed on an external monitor.

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ICON FUNCTION

Hourglass: Please wait while the system prepares for the next action.

Audio Recording is Active: Audio is being recorded on the video.

Note: The default for audio recording is OFF, so audio recording on the video
occurs only if the default has been changed to ON in user settings.

Back Arrow: Exit to previous screen.

Up Arrow: Select previous file for playback.

Down Arrow: Select next file for playback.

Play: Play the selected file or continue playing a paused video file.

Pause: Pause the video playback.

Snapshot: On the Playback menu, this icon indicates that a file is a snapshot.

Video: On the Playback menu, this icon indicates that a file is a video.

Figure 5. GlideScope Video Monitor Back Panel

Video‑out port:

Connect the
HDMI‑to‑DVI cable
from the external
monitor

USB port:

Connect a USB
flash drive to
record video or
take a snapshot

Power socket:

Connect the barrel
plug from the 12V
power adapter

Video cable port:
Attach the video cable

Product identification:
Includes product serial
number

Mounting plate:

Connect the monitor to a
mobile stand or IV pole

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SETTING UP

Please read the Warnings & Cautions section before performing the following tasks.

Before you can use the system for the first time, you must inspect the components, set up the system, and
perform a functional test as recommended by Verathon. Complete the following procedures:

1. Perform Initial Inspection—Inspect the system for any obvious physical damage that may have occurred
during shipment.

2. Mount the GlideScope Video Monitor (Optional)—Set up the GlideScope Video Monitor on a mobile
stand or IV pole.

3. Charge the Monitor Battery—You can use the system while the battery is charging.

Note: The monitor will operate without charging the battery by using the GlideScope Video Monitor 12V
DC Power Adapter that shipped with the unit.

4. Connect the Video Cable or Smart Cable to the Monitor—Attach the cable that connects the video
baton or laryngoscope to the monitor and transmits the video data.

5. Connect the Smart Cable to the Video Baton (VideoBaton2.0Only)—Attach the Smart Cable to a
GlideScope Video Baton 2.0.

6. Connect to an External Monitor (Optional)—Connect the monitor to an external display source, such as a
larger monitor screen, by using the HDMI‑to‑DVI cable.

7. Configure User Settings—Enter data customized to your clinic, and configure settings such as the date
and time.

8. Perform a Functional Check—Before you use the device for the first time, perform a functional check to
ensure that the system is working properly.

PROCedURe 1. PeRFORM INITIAL INSPeCTION

When you receive the system, Verathon recommends that an operator familiar with the instrument perform a
full visual inspection of the system for any obvious physical damage that may have occurred during shipment.

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. For contact information, visit verathon.com/global‑support.

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PROCedURe 2. MOUNT THe GLIdeSCOPe VIdeO MONITOR (OPTIONAL)

If you choose to mount the system, you may use either of the following configurations:

• Mount it on a premium cart or mobile stand (Figure 6 or Figure 7). These solutions make it easy for

you to move the system from one location to another.

• Mount it on an IV pole (Figure 8).

This procedure includes instructions for assembling the mobile stand, mounting the system on either the
mobile stand or an IV pole, and adjusting the monitor angle.

Figure 6. Premium Cart Figure 7. Mobile Stand Figure 8. IV Pole Mount

IV pole mount

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ATTACH THe MONITOR TO THe MOBILe STANd OR IV POLe

1. If you are using the GlideScope premium cart or AVL portable stand, assemble it according to the
instructions included with the component.

2. If you are using an IV pole mount, place the mounting bracket on the IV pole, and then tighten the
bracket attachment knob until the IV pole mount is secure.

Bracket attachment knob

3. On the mobile stand mount or the IV pole mount, ensure that the locking pin and quick‑release lever are
in the unlocked (horizontal) position.

Quick‑release lever
in unlocked position

Locking pin in
unlocked position

4. While holding the quick‑release locking plate with the head of the mounting screw facing away from
you and the larger of the two flanges to your left, Insert a positioning pin into the right‑hand hole on the
locking plate as shown in the following image.

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5. Using the orientation shown in the following images, screw the quick‑release locking plate to the back
panel of the monitor.

Quick‑release
locking plate

6. Seat the locking plate of the monitor on the quick‑release mount. When properly situated, the monitor sits
securely on the mount, and the quick‑release lever automatically snaps into the locked (down) position.

7. Ensure that the quick‑release lever is fully in the locked (down) position. This locks the monitor into place.

Quick‑release lever
in locked position

8. Adjust the locking pin to the locked (down) position. This secures the quick release lever in the locked position.

Locking pin in locked position

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AdJUST THe MONITOR ANGLe

Before you start using the video monitor, adjust the angle of the monitor for optimal viewing. The ideal angle
minimizes glare and maximizes visibility.

1. Turn the angle adjustment knob counterclockwise.

Angle

adjustment

knob

2. Tilt the monitor to the desired angle.

3. Turn the angle adjustment knob clockwise. This secures the monitor at the desired angle.

4. To attach a video baton cradle, see the procedure Attach the Video Baton Cradle (Optional).

PROCedURe 3. ATTACH THe VIdeO BATON CRAdLe (OPTIONAL)

You may elect to attach a video baton cradle to the mobile stand or IV pole mount.

1. Screw the center pole clamp to the video baton
cradle.

2. Attach the center pole clamp and video baton
cradle to the pole, and then turn the adjustment
knob clockwise to tighten.

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PROCedURe 4. CHARGe THe MONITOR BATTeRY

Please read the Warnings & Cautions section before performing the following task.

The GlideScope Video Monitor includes an internal lithium‑ion battery. Verathon recommends that you
charge the battery fully prior to first use.

Under normal operating conditions, a fully charged battery lasts approximately 90minutes or longer before it
needs to be recharged. For optimal battery life, ensure that the battery is fully charged before you try to use
the monitor in battery mode. You should charge the battery at temperatures between 0–35°C (32–95°F).

The percentage above the Battery Status icon indicates the remaining battery charge.

Figure 9. Battery Status Icons

19% battery life or less remaining. Battery must be charged.

20% to 50% battery life remaining.

51% to 82% battery life remaining.

Battery is 83% to fully charged. The lightning bolt indicates that the battery is charging.

1. Connect the video monitor 12V DC poweradapter to the power cable.

2. On the back panel of the monitor, remove the power socket cap, and then connect the 12V DC power
adapter to the power socket.

3. Plug the power supply into a hospital‑grade power outlet.

4. Allow the battery to charge. Fully charging the battery may take up to 6hours.

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PROCedURe 5. CONNeCT THe VIdeO CABLe OR SMART CABLe TO THe MONITOR

This procedure connects the video cable or Smart Cable to the monitor, which displays the image transmitted
from the camera.

Ensure that the video monitor is turned off prior to connecting or disconnecting the video cable or Smart
Cable.

1. Align the arrow on the video cable or Smart Cable and the arrow on the video cable port.

2. Insert the cable into the port. You will hear a click when the cable is successfully connected.

Note: When disconnecting the cable from the monitor, rotate the connector ring in the direction of the
arrow.

Connector ring

22

0900‑4200 REV‑11

PROCedURe 6. CONNeCT THe SMART CABLe TO THe VIdeO BATON

(VIdeOBATON2.0ONLY)

If you want to use GlideScope Video Batons 2.0 with the GlideScope Video Monitor, you can use a Smart
Cable to connect them.

Note: Video Batons 2.0 require system software version 3.9 or later. For more information, refer to System

Software on page37.

1. After connecting the Smart Cable to the monitor as described in the section Connect the Video Cable or

Smart Cable to the Monitor on page22, grasp the other end of the Smart Cable in one hand.

2. Holding the video baton in the other hand, align the HDMI connectors on the Smart Cable and the baton
with one another.

3. Insert the HDMI connector on the Smart Cable into the connector on the video baton.

4. Press the Smart Cable securely into place within the recess on the video baton.

Operations & Maintenance Manual: Setting up

23

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PROCedURe 7. CONNeCT TO AN eXTeRNAL MONITOR (OPTIONAL)

Please read the Warnings & Cautions section before performing the following task.

By using an HDMI‑to‑DVI cable, you can connect the GlideScope Video Monitor to an external monitor
that is approved for medical use. For more information, please contact your Verathon Customer Care
representative.

Note: Image quality on the external monitor may vary according the resolution of the external monitor.

Note: To maintain electromagnetic interference (EMI) within certified limits, the system must be used with
the cables, components, and accessories specified or supplied by Verathon. For additional information, see
the System Parts & Accessories and Component Specifications sections. The use of accessories or cables other
than those specified or supplied may result in increased emissions or decreased immunity of the system.

1. Ensure that the video monitor is turned off.

2. On the back of the monitor, remove the HDMI cap from the video‑out port.

3. Connect the HDMI end of the cable to the video‑out port.

Video‑out port

4. Connect the other end of the cable to the DVI port on an external monitor that is approved for medical
use.

5. Press the Power button. The monitor turns on.

6. Press the External Video button. The indicator LED to the right of the button illuminates when the
connection is successful, and the video displays on the external monitor.

7. To stop sending video to an external monitor, press the External Video button again.

8. Prior to disconnecting the HDMI‑to‑DVI cable, ensure the video monitor is turned off.

24

0900‑4200 REV‑11

PROCedURe 8. CONFIGURe USeR SeTTINGS

Mode Exit

GlideScope User Settings

Change Date, Time & Settings

01-15-2018 20:35:51 US

UBL Version: 1.4
Core Version: 3.4
Tutorial Version: 1.3
Baton Version:

Key Click Sound: OFF
Audio Recording: ON
Auto External Video: OFF
Clinic Name: CLINIC NAME

Auto Power Off: OFF
Auto Recording: OFF

Next Page

NOTE: PLUG IN POWER ADAPTER TO ENABLE SOFTWARE UPGRADING

UBoot Version: 2.1
Filesystem Version: 3.5
App Version: 3.9

+-

Scope

Power Cycle: 19

Running Time: 0 d 11 h 30 m

Back

GlideScope User Settings

Monitor

Power Cycle: 3

Running Time: 0 d 0 h 30 m

Battery Level: 94%

No USB Drive Detected.

Monitor
Download

Scope
Download

Blade

Power Cycle: 370

You may configure the following settings directly on the unit:

• Date and Time

• Date and Time Format

• Key Click Sound

• Auto Power Off

The second page of user settings, as seen in Figure 11, is only available if your GlideScope Video Monitor
is running software version 3.4 or higher. This page of user settings displays system use information, and it
does not contain any configurable settings. If you would like to update the software, see System Software on
page37.

• Audio Recording

• Auto Recording

• Auto External Video

• Clinic Name

Figure 10. User Settings Screen Page 1

Figure 11. User Settings Screen Page 2

1. If a USB flash drive is inserted into the monitor, remove it.

2. Press the Power button. The monitor turns on.

3. Press and hold the Tutorial button , and while continuing to hold it, press the Snapshot button .
The User Settings screen appears on the monitor. The configurable user settings are displayed in yellow,
and the selected setting is highlighted in red.

4. Customize your user settings by using the following buttons:

• Press the Record button to select the parameter you want to set.

• Press the Snapshot button to decrease the parameter value.

• Press the External Video button to increase the parameter value.

• When inputting the Clinic Name, the Tutorial button moves the selection to the next letter. Press

the Record button twice to return the selection back to the Date/Time setting.

• To view the second page of user settings, press the Record button until Next Page is highlighted

Operations & Maintenance Manual: Setting up

5. When you are finished customizing the settings, press the Record button until the option Exit is

in red, and then press the Tutorial button . To exit the second page of user settings, press the
Tutorial button again.

available in the gray bar, and then press the Tutorial button . This saves the parameters, and the User
Setting screen closes.

25

0900‑4200 REV‑11

PROCedURe 9. PeRFORM A FUNCTIONAL CHeCK

Before you use the device for the first time, perform the following functional check to ensure that the system
is working properly. Please contact your local Verathon representative or Verathon Customer Care if your
system does not function as described below. For contact information, visit verathon.com/global‑support.

ReQUIRed CHeCKS

1. Fully charge the monitor battery (this takes approximately 6hours).

2. Connect a video cable or Smart Cable to a video baton, and then connect it to the monitor.

3. Press the Power button. The monitor turns on.

4. Look at the monitor screen, and verify that the image displayed is being received from the video baton.

Note: There may be a slight blade intrusion in
the upper‑left and upper‑right corners of the
monitor, and a thin line may appear along the
top. These blade edges are captured in the
view because of the wide‑angle camera lens
used in the video laryngoscope. 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.

ReCOMMeNded CHeCKS

5. On the back of the monitor, remove the USB port cap, and then insert a USB flash drive into the port.

USB port

6. Ensure that the USB flash drive is detected by checking if the USB Flash Drive icon on the bottom of
the screen is displayed.

7. Press the Record button . Recording starts.

26

0900‑4200 REV‑11

8. To stop recording, press the Record button again.

9. Wait until the Saving File icon has disappeared from the screen, and then remove the USB flash drive
from the monitor.

10. On a computer, verify that the recorded video (.avi) file can be played.

Note:

If you are viewing the recorded file on a Windows operating system (OS), use an application such as
Windows Media Player.

If you are viewing the recorded video file on Mac OS, use an application such as one of the following:

• MPlayerX (free in the App Store)

• VLC (free at http://www.videolan.org/vlc/index.html)

If you are viewing the recorded video file on iOS, use an application such as one of the following:

• VLC for iOS (free in the App Store)

• 8player lite (free in the App Store)

• Media Player—PlayerXtreme HD (free in the App Store)

Operations & Maintenance Manual: Setting up

27

0900‑4200 REV‑11

USING THE DEVICE

Prior to using the device, set up the device according to the instructions in the previous chapter, and verify
the setup by completing the procedure Perform a Functional Check.

Please read the Warnings & Cautions section before performing the following tasks.

AVL video laryngoscopes are equipped with the Reveal anti‑fog feature, which reduces camera fogging
during the intubation procedure. To fully optimize the feature, you must allow the video laryngoscope to
warm up for 30‑120 seconds prior to use, depending on the ambient temperature and humidity of the
clinical environment. Full optimization of the anti‑fog feature is not necessary in order to use the device; if
desired, you may begin the intubation procedure immediately.

Note: If the video laryngoscope is stored in cold conditions, additional warming time may be required for
optimal performance of the anti‑fog feature.

Using the system consists of the following procedures:

• Connect the Video Cable or Smart Cable to the Monitor

• Insert the Video Baton into the Stat

• Prepare the GlideScope System

• Intubate Using a Video Baton and Stat

• Use the Record & Snapshot Features (Optional)

• Use the Playback Feature (Optional)

28

0900‑4200 REV‑11

PROCedURe 1. CONNeCT THe VIdeO CABLe TO THe MONITOR

Ensure that the video monitor is turned off prior to connecting or disconnecting the video cable.

1. Ensure the video laryngoscope and other system components have been properly cleaned and
disinfected. For more information, refer to the GlideScope and GlideRite Products Reprocessing Manual
(part number 0900‑5032).

2. Based on a clinical assessment of the patient and the experience and judgment of the clinician, select the
video baton/Stat combination that is appropriate for the patient.

3. Align the arrow on the video cable and the arrow on the video cable port.

4. Insert the video cable into the port. You will hear a click when the cable is successfully connected.

Note: When disconnecting the video cable from the monitor, rotate the connector ring in the direction of
the arrow.

Operations & Maintenance Manual: Using the Device

29

0900‑4200 REV‑11

PROCedURe 2. INSeRT THe VIdeO BATON INTO THe STAT

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

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.

PROCedURe 3. PRePARe THe GLIdeSCOPe SYSTeM

1. Press the Power button . The video monitor turns on.

Note: If the monitor locks up or becomes unresponsive for any reason, press and hold the Power button
for 10seconds to reboot the system.

2. Ensure that the battery is sufficiently charged. If necessary, connect the monitor directly to power.

3. On the monitor screen, verify that the image displayed is from the video laryngoscope camera. On the
monitor, a small portion of the GVL Stat may be visible on the top or upper‑left and right corners.

4. If needed, allow the GlideScope Reveal anti‑fog feature to warm up for 30–120seconds.

Note: The time required for the anti‑fog feature to be fully optimized varies according to the ambient
temperature and humidity where the equipment is being stored or used. If the video laryngoscope is
stored in cold conditions, additional warming time may be required for optimal performance of the
anti‑fog feature.

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.

* Compatibility has been demonstrated for up to one hour of continuous exposure on video batons and Stats.

30

0900‑4200 REV‑11

PROCedURe 4. INTUBATe USING A VIdeO BATON ANd STAT

Please read the Warnings & Cautions section before performing the following task.

To perform an intubation, Verathon recommends using the technique outlined in this procedure. Prior to
beginning this procedure, verify that the monitor is receiving an accurate image from the video laryngoscope.

1. Stabilize the patient’s head.

2. Look in the mouth, insert the blade midline, and then advance the tip into thevallecula.

3. Look at the screen, and then lift the epiglottis for a view of thelarynx.

4. Look in the mouth, and then introduce an endotracheal tube alongside theblade.

5. Look at the screen, and then complete theintubation.

6. If using a GlideRite Rigid Stylet, remove it by pulling toward the patient’sfeet.

Operations & Maintenance Manual: Using the Device

31

0900‑4200 REV‑11

PROCedURe 5. USe THe ReCORd & SNAPSHOT FeATUReS (OPTIONAL)

Please read the Warnings & Cautions section before performing the following tasks.

The system is equipped with video and audio recording features and the ability to save a snapshot of the
live display on the monitor. The video monitor saves this data to a USB flash drive, and you can view the
recordings or snapshots on a computer or on the video monitor. For more information about viewing these
files on a monitor, see Use the Playback Feature (Optional) on page34.

By default, audio recording is disabled on the system. If you would like the system to record audio in addition
to video, complete the procedure Configure User Settings in order to enter the User Setting display, and then
change the Audio Recording setting to On.

While recording, a number next to the icon indicates approximately what percentage of the USB flash drive
has been used. When the USB flash drive is full, recording stops.

1. On the back of the monitor, remove the USB port cap, and then insert a USB flash drive into the port.

Note: If you do not insert a USB flash drive, the video recording, audio recording, and snapshot features
will not be available.

USB port

2. Ensure that the USB flash drive is detected by checking if the USB Flash Drive icon on the bottom of
the screen is displayed.

3. If you are recording the intubation, press the Record button . Video recording starts and is saved to
the USB flash drive.

If audio recording is enabled in the User Settings display, the Audio Recording is Active icon will
appear on the screen, and audio will be recorded with the video.

4. When you are finished recording, press the Record button again, and then wait for the Saving File
icon to disappear.

Note: If you remove the USB flash drive before the Saving File icon disappears, the recording will be lost.

5. If at any point you would like to save a photo of the live display to the USB flash drive, press the

Snapshot button , and then wait for the Saving Snapshot icon to disappear.

Note: If you remove the USB flash drive before the Saving Snapshot icon disappears, the photo will be lost.

32

0900‑4200 REV‑11

6. If you would like to review the recorded files on the video monitor, complete the following procedure,

Use the Playback Feature (Optional).

If you would like to review the recorded files on a computer, insert the USB flash drive into the PC, and
then view the .avi or .jpg files.

Note:

If you are viewing the recorded file on a Windows operating system (OS), use an application such as
Windows Media Player.

If you are viewing the recorded video file on Mac OS, use an application such as one of the following:

• MPlayerX (free in the App Store)

• VLC (free at http://www.videolan.org/vlc/index.html)

If you are viewing the recorded video file on iOS, use an application such as one of the following:

• VLC for iOS (free in the App Store)

• 8player lite (free in the App Store)

• Media Player—PlayerXtreme HD (free in the App Store)

Operations & Maintenance Manual: Using the Device

33

0900‑4200 REV‑11

PROCedURe 6. USe THe PLAYBACK FeATURe (OPTIONAL)

20130411_213043.avi

20131101_132115.avi

20131101_132217.jpg

20130411_143605.avi

20140110_203355.avi

20140114_203419.avi

20140114_205213.jpg

Tutorial

Recorded videos and snapshots on a USB flash drive can be viewed on the GlideScope Video Monitor.

This feature is only available if your GlideScope Video Monitor is running software version 3.4 or higher. For
more information about upgrading the software, see System Software on page37.

1. On the back of the monitor, remove the USB port cap, and then insert a USB flash drive into the port.

2. Ensure that the USB flash drive is detected by checking if the USB Flash Drive icon on the bottom of
the screen is displayed.

3. Press and hold the Tutorial button 3 seconds or longer. The playback menu is displayed.

Figure 12. Playback Menu

4. Navigate the menu as follows:

5. When you have selected the item that you want to play, press the Tutorial button . Playback starts.

6. When the file is being played back and is displayed on the screen, press the Snapshot button to

7. If the file being played back is a video, pause and resume playback by pressing the Tutorial button .

8. Press the Record button to return to the playback menu.

9. Press the Record button again to close the playback menu.

• Press the Snapshot button to move up the list of playback files.

• Press the External Video button to move down the list of playback files.

playback the next file above the one currently displayed. Press the External Video button to play
the next file below the one currently displayed.

34

0900‑4200 REV‑11

TIPS FOR USING THE GLIDESCOPE AVL SYSTEM

• The GlideScope video laryngoscope is designed to be inserted down the midline of the tongue to the

epiglottis.

• Intubations using the GlideScope video laryngoscope only require approximately 0.5–1.5 kg (1–3.5 lbs)

of lifting force.

• The use of an endotracheal tube stylet is recommended. GlideRite stylets are designed to complement

the angle of the GlideScope video laryngoscope and facilitate intubation.

TIPS FOR WORKING WITH ENDOTRACHEAL TUBES

• Insert the ETT behind or immediately adjacent to the GlideScope video laryngoscope.

• Do not insert the stylet into the larynx during intubation.

• Carefully introduce the distal end of the ETT between the vocal folds.

• When introducing the video laryngoscope or the endotracheal tube, look directly into the mouth to

avoid damaging the endotracheal tube cuff, the patient’s teeth, or soft tissues such as the soft palate
or tonsils.

• Avoid excessive lifting or pushing of the glottis. Maximum laryngeal exposure may not facilitate

intubation; reducing the elevation applied to the laryngoscope may make inserting the ETT easier.

Operations & Maintenance Manual: Using the Device

35

0900‑4200 REV‑11

REPROCESSING

Some of the system components in this manual require cleaning between uses. In addition, some of
them require low‑level disinfection, high‑level disinfection, or sterilization between uses or under specific
circumstances. For information about the cleaning, disinfection, and sterilization requirements for these
components, refer to the GlideScope and GlideRite Products Reprocessing Manual (part number 0900‑5032),
which is available at verathon.com/product‑documentation.

36

0900‑4200 REV‑11

MAINTENANCE & SAFETY

PERIODIC INSPECTIONS

In addition to the user performing routine inspections before and after every use, periodic inspections should
be performed to ensure safe and effective operation. It is recommended that an operator familiar with the
instrument perform a full visual inspection of all components at least every three months. The inspector
should check the system for the following:

• External damage to the equipment

• Damage to the power supply or adapter

• Damage to the connectors or cable insulation

Report any suspected defects to Verathon Customer Care or your local representative. For contact information,
visit verathon.com/global‑support.

GLIDESCOPE VIDEO MONITOR BATTERY

Under normal operating conditions, the monitor battery will last 2–3 years; or approximately 500 charge/
discharge cycles. For more information about the battery, see the Component Specifications section on
page41.

The battery is not user‑replaceable. In case of battery malfunction, do not attempt to replace the monitor
battery. Any attempts to replace the battery by unauthorized service technicians may cause serious harm to
the user and will void the warranty. Please contact your Verathon Customer Care Representative for more
information on battery replacement.

SYSTEM SOFTWARE

Verathon may release software upgrades for the GlideScope Video Monitor. Software upgrades are supplied
directly by Verathon or an authorized representative, and installation instructions are provided with the
upgrade.

This manual documents the most current version of the GlideScope Video Monitor software. If your monitor
does not function as described in this manual, or to determine if your software should be updated, contact
Verathon Customer Care.

Do not perform any software upgrades from third‑party vendors or attempt to modify the existing software.
Doing so may damage the monitor and void the warranty.

Operations & Maintenance Manual: Maintenance & Safety

37

0900‑4200 REV‑11

DEVICE REPAIR

The system components are not user‑serviceable. Verathon does not make available any type of circuit
diagrams, component parts lists, descriptions, or other information that would be required for repairing the
device and related accessories. All service must be performed by a qualified technician.

If you have any questions, contact your local Verathon representative or Verathon Customer Care.

Please read the Warnings & Cautions section.

DEVICE DISPOSAL

Disposal of this device in accordance with WEEE requirements can be coordinated through your Verathon
Service Center.

38

0900‑4200 REV‑11

WARRANTY

ORIGINAL TOTAL CUSTOMER CARE WARRANTY

This Limited Warranty (“Warranty”) is provided by Verathon Inc. (“Verathon”) to its customer, distributor,
original equipment manufacturer, end‑user, or other purchaser (“Buyer”) on the terms and conditions stated
herein, for the GlideScope product (“Product”). The terms of this Warranty are subject to the standard Terms
and Conditions of Sale or any other separate negotiated agreement between the parties.

SCOPE OF COVERAGE: This Warranty covers service and repair of all malfunctions (mechanical, electrical,
and other defects) associated with the Product purchased by Buyer from Verathon, including coverage for
accidental drops or mishandling of Product (subject to Buyer’s payment of a deductible charge for Product
replacement), for a period of one (1) year (unless otherwise noted under “COVERED COMPONENTS” below)
from Product shipment date (“Term”), and applies only to the original Buyer. Replacement parts will be new,
rebuilt or non‑original manufacturer’s parts that perform to the factory specifications of the Product at
Verathon’s sole option.

Verathon will perform repair and replacement services (“Service”) only on Products purchased from an
authorized dealer. If the Product or component is purchased from an unauthorized dealer, or if the original
factory serial number has been removed, defaced or altered, this Warranty is void.

If a Product purchased by Buyer requires Service, Verathon will, at its discretion, either repair or replace the
Product and may provide a loaner unit, at Buyer’s request. If Buyer requests a loaner unit, Buyer shall send
the defective Product to Verathon (cleaned and disinfected as appropriate) immediately upon receiving the
loaner unit from Verathon. Buyer shall return the loaner unit within two (2) business days of receipt of the
repaired Product. All exchanged parts become property of Verathon.

EXCLUSIONS: This Warranty excludes problems caused by the Buyer’s acts (or failure to act), the acts of
others, or events beyond Verathon’s reasonable control including:

• Accident, theft, misuse, abuse, extraordinary wear and tear, or neglect.

• Misapplication, improper use, or other failure to follow Verathon’s product instructions and safety

precautions contained in the Operations and Maintenance Manual. This warranty does not apply if
there is evidence of the equipment being exposed to temperatures in excess of 60°C (140°F).

• Use of the system in conjunction with hardware, software, components, services, accessories,

attachments, interfaces, or consumables, other than those supplied or specified by Verathon.

• Products that have been repaired or maintained by anyone other than a Verathon authorized service

provider.

• Modification, disassembly, rewiring, re‑engineering, recalibration, and/or reprogramming of Products

other than as specifically authorized by Verathon in writing.

COVERED COMPONENTS: Warranty coverage applies to the following components:

• GlideScope Video Monitor

• GlideScope AVL Video Baton

• GlideScope Video Baton 2.0 (two‑year factory warranty)

• GlideScope Spectrum Smart Cable (two‑year factory warranty)

Additional reusable components purchased either singularly or as a part of a system, including GlideScope
Workstations and the GlideScope Video Cable, are limited to a one‑year factory warranty unless stated
otherwise. Consumable items are not covered under this warranty.

Operations & Maintenance Manual: Warranty

39

0900‑4200 REV‑11

EXTENDED WARRANTIES: Buyer may purchase a Premium Total Customer Care warranty that extends
this Limited Warranty. For more information, contact Verathon’s Customer Care Department or your local
representative.

LIMITED REMEDY: This Warranty gives Buyer specific legal rights which may vary based on local law. When,
under applicable law, implied warranties are not allowed to be excluded in their entirety, such warranties will
be limited to the duration of the applicable written warranty and, for European Customers, any terms herein
limiting Verathon’s liability shall not apply insofar as they conflict with mandatory statutory provisions of the
Product Liability Act.

TO THE FULL EXTENT ALLOWED BY LAW, THE FOREGOING LIMITED WARRANTIES AND REMEDIES
ARE EXCLUSIVE AND EXPRESSLY IN LIEU OF ALL OTHER WARRANTIES, REPRESENTATIONS, TERMS,
OR CONDITIONS, WRITTEN OR ORAL, EXPRESS OR IMPLIED, STATUTORY OR OTHERWISE, INCLUDING
BUT NOT LIMITED TO ANY WARRANTIES, TERMS OR CONDITIONS OF MERCHANTABILITY OR FITNESS
FOR A PARTICULAR PURPOSE, SATISFACTORY QUALITY, CORRESPONDENCE WITH DESCRIPTION, AND
NON‑INFRINGEMENT, ALL OF WHICH ARE HEREBY EXPRESSLY DISCLAIMED.

TRANSFER OF SERVICE: This Warranty extends only to Buyer, and may not be transferred to third parties by
operation of law or otherwise.

40

0900‑4200 REV‑11

PRODUCT SPECIFICATIONS

COMPONENT SPECIFICATIONS

Table 4. GlideScope Video Monitor (0570‑0338)

GENERAL SPECIFICATIONS

Classification: Electrical Class II, Applied Part BF

Line voltage:

DC power supply: 12 V DC, 3.33 A max
Ingress protection: IP54

Temperature: 10–40°C (50 –104°F) ‑20– 45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440‑1060 hPa

Range: 100–240 VAC, 50 and 60 Hz. Connect to a medical‑grade power supply (If
the provided power cord has a third prong, it is used as a functional ground).

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions

COMPONENT SPECIFICATIONS

Shipping & Storage

Conditions

Screen type and
resolution

Screen size
(diagonal;A)

Height (B) 174 mm

Width (C) 223 mm

Depth (D) 80 mm

Weight 1.0 kg

TFT Color
VGA 640 × 480 px

16.3cm (6.4 in)

A

B

C

D

Operations & Maintenance Manual: Product Specifications

41

0900‑4200 REV‑11

Table 5. Spectrum Smart Cable (0800‑0543)

GENERAL SPECIFICATIONS

Ingress protection: IPX8

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20– 45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440‑1060 hPa

COMPONENT SPECIFICATIONS

Length (A) 1417 ± 25mm

A

Diameter (B) 6.8 mm

B

Table 6. Premium Cart (0800‑0537)

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20– 45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440‑1060 hPa

COMPONENT SPECIFICATIONS

Wheelbase diameter(A) 53.3 cm

Minimum height (B) 101.6 cm

B–C

Maximum height (C) 132.1 c m

Weight 8.0–8.4kg

42

0900‑4200 REV‑11

A

Table 7. Mobile Stand (0800‑0410)

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20– 45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440‑1060 hPa

COMPONENT SPECIFICATIONS

Wheelbase diameter(A) 61 cm

B–C

Minimum height (B) 76 cm

Maximum height (C) 122 cm

A

Table 8. IV Pole Mount (0810‑0200)

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20– 45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440‑1060 hPa

COMPONENT SPECIFICATIONS

Arm length (A) 27 cm

Width (B) 6.3 cm

Pole width range (C) 6.4–33 mm

B

Weight 0.9 kg

A

C

Operations & Maintenance Manual: Product Specifications

43

0900‑4200 REV‑11

Table 9. AVL Video Baton 1‑2 (0570‑0306)

GENERAL SPECIFICATIONS

Ingress protection: IPX8
Expected product life: 2 years or 1000 cycles

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20–45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440 ‑10 60 hPa

COMPONENT SPECIFICATIONS

Length of flexible portion of baton
(A)

66.0mm

D

Height at camera (B) 6.0mm

Width at camera (C) 7.0mm

Video cable length (D) 2041 ± 50mm

Field of view (E) 41°

Direction of view 0°

A

Cable shortened for illustrative purposes

B

C

E

Table 10. AVL Video Baton 3‑4 (0570‑0307)

GENERAL SPECIFICATIONS

Ingress protection: IPX8
Expected product life: 2 years or 1000 cycles

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20–45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440 ‑10 60 hPa

COMPONENT SPECIFICATIONS

Length of flexible portion of baton
(A)

105.0mm

D

Height at camera (B) 11mm

Width at camera (C) 11mm

Video cable length (D) 1540 ± 50mm

Field of view (E) 49°

Direction of view 0°

A

Cable shortened for illustrative purposes

B

C

E

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0900‑4200 REV‑11

Table 11. AVL Video Baton 2.0 Large (3‑4; 0570‑0382)

GENERAL SPECIFICATIONS

Ingress protection: IPX8
Expected product life: 2 years or 2000 cycles

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20–45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 440 ‑10 60 hPa

COMPONENT SPECIFICATIONS

Length of flexible portion of baton
(A)

105.0mm

Height at camera (B) 11mm

Width at camera (C) 11mm

Field of view (D) 49°

A

B

Direction of view 0°

C

D

Table 12. GVL Stat 0 (0574‑0104)

GENERAL SPECIFICATIONS

Expected product life:

Refer to the “use by” date indicated by the symbol on the package label.

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) 0–45°C (32–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 800–1060 hPa

COMPONENT SPECIFICATIONS

Height at camera (A) 8.6mm

Blade tip to handle (B) 36.2mm

Width at camera (C) 11.0mm

Blade length in front of camera (D) 6.5 mm

Max blade width in front of camera
(E)

11. 0 mm

A

B
F

D

Insertion portion (IP) length (F) 42 mm

Insertion portion (IP) width 15 mm

C

E

Operations & Maintenance Manual: Product Specifications

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0900‑4200 REV‑11

Table 13. GVL Stat 1 (0574‑0026)

GENERAL SPECIFICATIONS

Expected product life:

Refer to the “use by” date indicated by the symbol on the package label.

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) 0–45°C (32–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 800–1060 hPa

COMPONENT SPECIFICATIONS

Height at camera (A) 8.6mm

Blade tip to handle (B) 43.5mm

Width at camera (C) 10.1mm

Blade length in front of camera (D) 15.0mm

Max blade width in front of camera
(E)

12.7mm

A

B

F

D

Insertion portion (IP) length (F) 50 mm

Insertion portion (IP) width 15 mm

Table 14. GVL Stat 2 (0574‑0027)

C

E

GENERAL SPECIFICATIONS

Expected product life:

Refer to the “use by” date indicated by the symbol on the package label.

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) 0–45°C (32–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 800–1060 hPa

COMPONENT SPECIFICATIONS

Height at camera (A) 8.6mm

Blade tip to handle (B) 55.7mm

Width at camera (C) 11.2mm

Blade length in front of camera (D) 28.0mm

Max blade width in front of camera
(E)

16.0mm

A

B

F

D

Insertion portion (IP) length (F) 62 mm

Insertion portion (IP) width 18 mm

C

E

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0900‑4200 REV‑11

Table 15. GVL Stat 2.5 (0574‑0110)

GENERAL SPECIFICATIONS

Expected product life:

Refer to the “use by” date indicated by the symbol on the package label.

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) 0–45°C (32–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 800–1060 hPa

COMPONENT SPECIFICATIONS

Height at camera (A) 9.1mm

Blade tip to handle (B) 63.4mm

Width at camera (C) 12.7mm

Blade length in front of camera (D) 37.0mm

Max blade width in front of camera
(E)

19.7mm

A

B

F

D

Insertion portion (IP) length (F) 74 mm

Insertion portion (IP) width 22 mm

E

C

Table 16. GVL Stat 3 (0574‑0100)

GENERAL SPECIFICATIONS

Expected product life:

Refer to the “use by” date indicated by the symbol on the package label.

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20–45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 595–1060 hPa

COMPONENT SPECIFICATIONS

Height at camera (A) 14.3mm
Blade tip to handle (B) 72.5mm
Width at camera (C) 16.0mm
Blade length in front of camera (D) 37.0mm
Max blade width in front of camera

(E)

19.7mm

A

B

F

D

Insertion portion (IP) length (F) 89 mm
Insertion portion (IP) width 25 mm

C

E

Operations & Maintenance Manual: Product Specifications

47

0900‑4200 REV‑11

Table 17. GVL Stat 4 (0574‑0101)

GENERAL SPECIFICATIONS

Expected product life:

Refer to the “use by” date indicated by the symbol on the package label.

OPERATING & STORAGE SPECIFICATIONS

Operating Conditions Shipping & Storage Conditions

Temperature: 10–40°C (50 –104°F) ‑20–45°C (‑4–113°F)
Relative humidity: 10–95% 10–95%
Atmospheric pressure: 700–1060 hPa 595–1060 hPa

COMPONENT SPECIFICATIONS

Height at camera (A) 14.3mm
Blade tip to handle (B) 87.0mm
Width at camera (C) 20.3mm
Blade length in front of camera (D) 52.0mm
Max blade width in front of camera

(E)

27.5mm

A

B

F

D

Insertion portion (IP) length (F) 105 mm
Insertion portion (IP) width 30 mm

C

E

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BATTERY SPECIFICATIONS

Table 18 . Battery Specifications

CONDITION DESCRIPTION

Battery type Lithium‑ion

Battery life

Charging time

Rated capacity 2150mAh
Nominal voltage 7.2V
Max charging voltage 8.4V
Nominal weight 90g (3.17oz)
Width 23mm (0.9in)
Length 391mm (5.4in)
Thickness 23mm (0.9in)

Under normal operating conditions, a fully charged battery lasts approximately
90minutes

Charging time off line will take no more than 6hours from an empty battery to
a full charge

Operations & Maintenance Manual: Product Specifications

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0900‑4200 REV‑11

ELECTROMAGNETIC COMPATIBILITY

The system is designed to be in compliance with IEC60601‑1‑2, which contains electromagnetic compatibility
(EMC) requirements for medical electrical equipment. The limits for emissions and immunity specified in this
standard are designed to provide reasonable protection against harmful interference in a typical medical
installation.

The system complies with the applicable essential performance requirements specified in IEC60601‑1
and IEC60601‑2‑18. Results of immunity testing show that the essential performance of the system is not
affected under the test conditions described in the following tables. For more information about the essential
performance of the system, see Essential Performance on page1.

ELECTROMAGNETIC EMISSIONS

Table 19. Guidance and Manufacturer’s Declaration—Electromagnetic Emissions

The system is intended for use in the electromagnetic environment specified below. The customer or the user
of the system should ensure that it is used in such an environment.

EMISSIONS TEST COMPLIANCE ELECTROMAGNETIC ENVIRONMENT – GUIDANCE

RF emissions
CISPR 11

RF emissions
CISPR 11

Harmonic emissions
IEC61000‑3‑2

Voltage fluctuations/
flicker emissions
IEC61000‑3‑3

Group 1

Class A

Class A

In compliance

The system uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.

The system is suitable for use in all establishments other than
domestic and those directly connected to the public low‑voltage
power supply network that supplies buildings used for domestic
purposes.

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ELECTROMAGNETIC IMMUNITY

Table 20. Guidance and Manufacturer’s Declaration —Electromagnetic Immunity

The system is intended for use in the electromagnetic environment specified below. The customer or the user
of the system should ensure that it is used in such an environment.

IMMUNITY TESTS IEC60601 TEST LEVEL

Electrostatic discharge
(ESD)

IEC61000‑4‑2

Electrical fast transient/
burst

IEC61000‑4‑4

Surge

IEC61000‑4‑5

± 8kV contact

± 15kV air

± 2kV for power
supplylines

100 kHz repetition
frequency

± 1kV line(s) to line(s)

± 2kV line(s) to earth

0% UT; 0.5 Cycle
Voltage dips, short
interruptions and
voltage variations on
power supply input lines

IEC61000‑4‑11

At 0˚, 45˚, 90˚, 135˚, 180˚,

225˚, 270˚, and 315˚

0% UT; 1 cycle and 70%

UT; 25/30 cycles

Single Phase: at 0˚

Rated power frequency
magnetic fields

30 A/m

Frequency 50/60 Hz
IEC61000‑4‑8

3Vrms

150kHz to 80MHz
Conducted RF

6 Vrms in ISM bands
IEC61000‑4‑6

150 kHz to 80 MHz

80% AM at 1 kHz

COMPLIANCE

LEVEL

In compliance

In compliance

In compliance

In compliance

In compliance

In compliance

ELECTROMAGNETIC ENVIRONMENT

– GUIDANCE

Floors should be wood, concrete,
or ceramic tile. If floors are covered
with synthetic material, the relative
humidity should be at least 30%.

Mains power quality should be that
of a typical hospital environment.

Mains power quality should be that
of a typical hospital environment.

Mains power quality should be that
of a typical hospital environment.
If the user of the system requires
continued operation during
power mains interruptions, it is
recommended that the system be
powered from an uninterruptible
power supply or a battery.

Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
hospital environment.

Portable and mobile RF
communications equipment
should be used no closer to any
part of the system, including
cables, than the recommended
separation distance calculated from
the equation applicable to the
frequency of the transmitter.

Recommended separation
distance d (m)

Operations & Maintenance Manual: Product Specifications

d=1.2 √P

51

0900‑4200 REV‑11

Table 20. Guidance and Manufacturer’s Declaration —Electromagnetic Immunity

The system is intended for use in the electromagnetic environment specified below. The customer or the user
of the system should ensure that it is used in such an environment.

IMMUNITY TESTS IEC60601 TEST LEVEL

Radiated RF

3V/m

80MHz to 2.7GHz
IEC61000‑4‑3

80% AM at 1 kHz

COMPLIANCE

In compliance

Note: Ut is the AC mains voltage prior to application of the test level.

These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.

ACCESSORY CONFORMANCE TO STANDARDS

To maintain electromagnetic interference (EMI) within certified limits, the system must be used with the
cables, components, and accessories specified or supplied by Verathon. For additional information, see the

System Parts & Accessories and Component Specifications sections. The use of accessories or cables other

than those specified or supplied may result in increased emissions or decreased immunity of the system.

Table 21. EMC Standards for Accessories

LEVEL

ELECTROMAGNETIC ENVIRONMENT

– GUIDANCE

Interference may occur in the
vicinity of equipment marked with
the following symbol:

ACCESSORY LENGTH

AC power cord 4.5m (15.0ft)
DC medical power adapter cable 2.5 m (8.2 ft)
HDMI‑to‑DVI cable 4.6m (15.1ft)
Smart Cable 1.6m (5.2ft)

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GLOSSARY

The following table provides definitions for specialized terms used in this manual or on the product itself. For
a full list of caution, warning, and informational symbols used on this and other Verathon products, please
refer to the Verathon Symbol Glossary (part number 0900‑4757) at verathon.com/symbols.

TERM DEFINITION

A Ampere
AC Alternating current
C Celsius
CFR Code of Federal Regulations (U.S.)
CISPR International Special Committee on Radio Interference
cm Centimeter
DC Direct current
DL Direct laryngoscopy
ED Emergency Department
EMI Electromagnetic interference
ESD Electrostatic discharge
Essential performance The system performance necessary to achieve freedom from unacceptable risk
ETT Endotracheal tube
F Fahrenheit
g Gram
GHz Gigahertz
HDMI High‑definition multimedia interface
hPa Hectopascal
Hz Hertz
ICU Intensive Care Unit
IEC International Electrotechnical Commission
in Inch
IPA Isopropyl alcohol
ISM Industrial, scientific, and medical
kHz Kilohertz
kV Kilovolt
lbs Pounds
m Meter
mAh Milliampere‑hour
MHz Megahertz
mm Millimeter
NICU Neonatal Intensive Care Unit
OR Operating Room

Operations & Maintenance Manual: Glossary

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TERM DEFINITION

OSHA Occupational Safety and Health Administration (federal agency in U.S.)
oz Ounce
ppm Parts per million
RF Radio frequency
RH Relative humidity
V Volt
Vrms Voltage root mean squared
WEEE Waste electrical and electronic equipment

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