Verathon GlideScope System AVL Single-Use Manual

GLIDESCOPE SYSTEM
AVL SINGLE‑USE
Operations & Maintenance Manual

0900‑4200 REV‑10

GLIDESCOPE SYSTEM
AVL SINGLE‑USE
Operations & Maintenance Manual
Effective: June 2, 2020
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
0413
Copyright © 2020 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.

i
Operations & Maintenance Manual: Table of Contents
0900‑4200 REV‑10
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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0900‑4200 REV‑10
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

1
Operations & Maintenance Manual: Important Information
0900‑4200 REV‑10
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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0900‑4200 REV‑10
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
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.
WARNING

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Operations & Maintenance Manual: Important Information
0900‑4200 REV‑10
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.
WARNING

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0900‑4200 REV‑10
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
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
immunity. This may cause improper operation, procedure delays, or both.
WARNING
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
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.
WARNING