Verathon GlideScope Manual

GLIDESCOPE SYSTEM
AVL SINGLE‑USE
Operations & Maintenance Manual

0900‑4200‑08‑60

GLIDESCOPE SYSTEM
AVL SINGLE‑USE
Operations & Maintenance Manual
Effective: August 27, 2018
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/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]
0413
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.
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.
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.

i
Operations & Maintenance Manual: Table of Contents
TABLE OF CONTENTS
IMPORTANT INFORMATION.................................................................................................................................1
Product Information............................................................................................................................................1
Statement of Intended Use..................................................................................................................................1
Essential Performance .........................................................................................................................................1
Statement of Prescription ....................................................................................................................................1
Notice to All Users ..............................................................................................................................................1
Precautions & Warnings ......................................................................................................................................2
Product Description ............................................................................................................................................7
INTRODUCTION ..................................................................................................................................................10
System Parts & Accessories ...............................................................................................................................10
Language Settings ............................................................................................................................................ 12
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 (Single‑Use Only)...........................................................30
Procedure 3. Prepare the GlideScope System............................................................................................30
Procedure 4. Intubate Using a Video Baton and Stat ................................................................................. 31
Procedure 5. Intubate Using the GlideScope Direct ...................................................................................32
Procedure 6. Use the Record & Snapshot Features (Optional) ....................................................................33
Procedure 7. Use the Playback Feature (Optional) .....................................................................................34
CLEANING & DISINFECTING ...............................................................................................................................36
General Information..........................................................................................................................................36
Procedure 1. Clean the GlideScope Video Monitor....................................................................................40
Procedure 2. Clean the Power Adapter.....................................................................................................40
Procedure 3. Clean the Cradle ..................................................................................................................40
Procedure 4. Clean the GlideScope Premium Cart..................................................................................... 41
Video Batons ....................................................................................................................................................41
Procedure 5. Remove the Stat .................................................................................................................. 41
Procedure 6. Clean & Disinfect the Video Baton .......................................................................................42
Procedure 7. Inspect the Video Baton.......................................................................................................45
Procedure 8. Clean the Smart Cable .........................................................................................................46
Procedure 9. Disinfect the Smart Cable.....................................................................................................50
Procedure 10. Sterilize the Smart Cable (Optional) ......................................................................................53
Direct Intubation Trainer ...................................................................................................................................54
Procedure 11. Clean & Disinfect the GlideScope Direct ...............................................................................54
MAINTENANCE & SAFETY..................................................................................................................................56
Periodic Inspections ..........................................................................................................................................56
GlideScope Video Monitor Battery ....................................................................................................................56
System Software...............................................................................................................................................56
Device Repair....................................................................................................................................................57
Device Disposal.................................................................................................................................................57

iii
Operations & Maintenance Manual: Table of Contents
WARRANTY.........................................................................................................................................................58
PRODUCT SPECIFICATIONS.................................................................................................................................60
System Specifications........................................................................................................................................60
Component Specifications ................................................................................................................................61
Battery Specifications........................................................................................................................................68
Electromagnetic Compatibility...........................................................................................................................69
GLOSSARY ...........................................................................................................................................................73

1
Operations & Maintenance Manual: Important Information
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.
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

2
PRECAUTIONS & 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.
PRECAUTIONS
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69.
To maintain electromagnetic interference (EMI) within certified limits, the GlideScope system
must be used with the cables, components, and accessories specified or supplied by Verathon®.
For additional information, see the System Parts & Accessories and Product 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.
The GlideScope system should not be used adjacent to or stacked with other equipment. If
adjacent or stacked use is necessary, the system should be observed to verify normal operation
in the configuration in which it will be used.
This device can radiate radio frequency energy and is very 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.
CAUTION
The system contains electronics that could be damaged by ultrasonic and automated washing
equipment. Do not use an ultrasonic device or automated washing equipment to clean this
product.
CAUTION

3
Operations & Maintenance Manual: Important Information
When cleaning video laryngoscopes, do not use metal brushes, abrasive brushes, scrub pads, or
rigid tools. They will scratch the surface of the unit or the window protecting the camera and
light, which may permanently damage the device.
CAUTION
Bleach may be used on the video batons, but pay special attention to stainless steel
components, as bleach can corrode stainless steel.
CAUTION
Ensure that you do not use any abrasive substances, brushes, pads, or tools when cleaning the
video monitor screen. The screen can be scratched, permanently damaging the device.
CAUTION
Risk of permanent equipment damage. This product is sensitive to heat, which will cause
damage to the electronics. Do not expose the system to temperatures above 60°C (140°F),
and do not use autoclaves or pasteurizers. Use of such methods to clean, disinfect, or sterilize
the system will cause permanent device damage and void the warranty. For a list of approved
cleaning procedures and products, see the Cleaning & Disinfecting chapter.
CAUTION
WARNINGS
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

4
If the GlideScope Direct is powered on for an extended period of time, it is possible for the
surface temperature to exceed 41°C (106°F) at the tip of the blade, where the lighting and
camera are located.
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 video monitor screen. Failure to do so
may result in injury, such as to the tonsils or soft palate.
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. 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/support.
WARNING
GlideScope systems are delivered nonsterile and require cleaning or disinfection prior to initial use.
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
Ensure that you follow the manufacturer’s instructions for handling and disposing of the
cleaning, disinfection, or sterilization solutions provided in this manual.
WARNING
Availability of cleaning, disinfection, and sterilization products varies by country, and Verathon
is unable to test products in every market. For more information, please contact Verathon
Customer Care. For contact information, visit verathon.com/support.
WARNING

5
Operations & Maintenance Manual: Important Information
This product may only be cleaned, disinfected, or sterilized by using the approved
low‑temperature processes provided in this manual. Cleaning, disinfection, and sterilization
methods listed are recommended by Verathon based on efficacy or compatibility with
component materials.
WARNING
Cleaning is critical to ensuring a component is ready for disinfection or sterilization. Failure
to properly clean the device could result in a contaminated instrument after completing the
disinfection or sterilization procedure.
When cleaning, ensure all foreign matter is removed from the surface of the device. This allows
the active ingredients of the chosen disinfection method to reach all the surfaces.
WARNING
Do not place the video baton in the cradle if any of the components are contaminated.
WARNING
In order to maintain electrical safety, use only the provided, medical‑approved power supply.
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 will void the warranty. Contact
Verathon Customer Care for all servicing needs.
WARNING
No modification of this equipment is allowed.
WARNING

6
The external monitor must be safety‑approved medical equipment.
WARNING
Use only a passive‑type USB flash drive. Do not use USB drives powered by another
externalsource.
WARNING
When cleaning the power adapter, use a cloth dampened with isopropyl alcohol on the outside
of the enclosure. Do not immerse the power adapter in water.
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

7
Operations & Maintenance Manual: Important Information
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 AVL video batons and GlideScope Direct blade connect directly to a full‑color,
digital video monitor for real‑time viewing.
The system is recommended for use with an endotracheal tube stylet, particularly the GlideRite®Rigid Stylet,
which complements the blade angle. For more information about the stylet, see the GlideRite Rigid Stylet
Operations and Maintenance Manual.
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

8
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 ranging in size from preterm infants to large adults.
The system may include the following components:
• GlideScope Video Monitor
• AVL Video Baton 1‑2 (for neonatal patients and small children)
○GVL 0 Stat, for patients less than 1.5 kg (3.3lbs)*
○GVL 1 Stat, for patients between 1.5–3.8 kg (3.3–8.4lbs)*
○GVL 2 Stat, for patients between 1.8–10 kg (4–22lbs)*
○GVL 2.5 Stat, for patients between 10–28 kg (22–61.7lbs)*
• AVL Video Baton 3‑4 (for use on children and adults)
○GVL 3 Stat, for patients between 10 kg–adult (22lbs–adult)*
○GVL 4 Stat, for patients between 40 kg–large adult (88.2lbs–large adult)*
• Video Baton 2.0 Large (3‑4, for use on children and adults)
○GVL 3 Stat, for patients between 10 kg–adult (22lbs–adult)*
○GVL 4 Stat, for patients between 40 kg–large adult (88.2lbs–large adult)*
• GlideRite®Rigid Stylet (recommended for use with the AVL Video Baton 3‑4 or Video Baton 2.0 Large)
* Weight ranges are approximate; a medical professional must evaluate on a patient‑by‑patient basis.
Note: Video Batons 2.0 require system software version 3.9 or later. For more information, refer to System
Software on page56.
Figure 2. GlideScope AVL Single‑Use System

9
Operations & Maintenance Manual: Important Information
GLIDESCOPE DIRECT INTUBATION TRAINER
The GlideScope Direct intubation trainer is designed to work with the GlideScope Video Monitor. The
GlideScope Direct resembles a traditional Macintosh direct laryngoscope with the addition of a video camera
near the end of the blade, permitting both direct laryngoscopy and a video display of the airway. This
provides the user with a laryngeal view, permits mentoring by an instructor, and combined with the system
monitor allows the image to be captured for documentation, quality control, and teaching.
The GlideScope Direct intubation trainer does not provide the same benefits of GlideScope video
laryngoscopes in settings when a line‑of‑sight cannot be achieved. Typically, these occur in patients
with difficult (Cormack‑Lehane grade 3 or 4) airways. It will, however, facilitate the instruction of direct
laryngoscopy. Should the GlideScope Direct fail to provide an adequate laryngeal view, the airway manager
can easily convert to a single‑use video baton and GVL®Stat for an optimal view.
Figure 3. GlideScope Direct Intubation Trainer

10
INTRODUCTION
SYSTEM PARTS & ACCESSORIES
The system consists of the following components.
Table 1. System Components
PARTS & ACCESSORIES
Required Components
GlideScope Video Monitor Video batons (for Single‑Use system only)
GVL®Stat sizes 0, 1, 2, 2.5, 3, and 4 (for Single‑Use system only)
Smart Cable
(for Video Baton 2.0)
Note: Cable shortened for
illustrationpurposes.
Video monitor 12V DC
poweradapter
Power cable

11
Operations & Maintenance Manual: Introduction
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
GlideScope Direct IV pole mounting kit HDMI‑to‑DVI cable
GlideRite®DLT Stylet
Note: For ET tubes 6.0mm orlarger
GlideRite Rigid Stylet
Note: For ET tubes 6.0mm orlarger
GlideRite Single‑Use Stylet (Small)
Note: For ET tubes 3.0–4.0mm

12
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/support.
VIDEO LARYNGOSCOPE COMPONENTS
Figure 4. Single‑Use Video Laryngoscope Components
Camera and light
Single‑use Stat
Video baton
Video cable
Smart Cable
Figure 5. GlideScope Direct Intubation Trainer
Video cable
(Shortened for illustration)
Connector
(Attaches to the monitor)
Cleaning cap Camera and light
Lifter blade
Handle