Verathon GlideScope, GlideScope System AVL Single-Use Operation & Maintenance Manual

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GLIDESCOPE SYSTEM

AVL SINGLE‑USE

Operations & Maintenance Manual

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0900‑4200‑08‑60

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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).

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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: +1 800 331 2313 (US and Canada only)

Tel: +1 425 867 1348

Fax: +1 425 883 2896

verathon.com

Verathon Medical (Europe) B.V.

Willem Fenengastraat 13

1096 BL Amsterdam

The Netherlands

Tel: +31 (0) 20 210 30 91

Fax: +31 (0) 20 210 30 92

Verathon Medical (Canada) ULC

2227 Douglas Road

Burnaby, BC V5C 5A9

Canada

Tel: +1 604 439 3009

Fax: +1 604 439 3039

0413

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.

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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

Operations & Maintenance Manual: Table of Contents

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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

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WARRANTY.........................................................................................................................................................58

PRODUCT SPECIFICATIONS .................................................................................................................................60

System Speciﬁcations ........................................................................................................................................ 60

Component Speciﬁcations ................................................................................................................................61

Battery Speciﬁcations ........................................................................................................................................68

Electromagnetic Compatibility ........................................................................................................................... 69

GLOSSARY ...........................................................................................................................................................73

Operations & Maintenance Manual: Table of Contents

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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.

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

Operations & Maintenance Manual: Important Information

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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

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 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.

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CAUTION

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.

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.

Operations & Maintenance Manual: Important Information

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WARNING

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.

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WARNING

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.

Operations & Maintenance Manual: Important Information

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WARNING

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.

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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 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

Operations & Maintenance Manual: Important Information

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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 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

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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

Operations & Maintenance Manual: Important Information

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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 (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

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PARTS & ACCESSORIES

Optional Components

Premium cart

Mobile stand

Media storage USB ﬂash

Universal accessory basket

Note: For use with AVL portablestand

Cradle for video baton

drive

GlideScope Direct IV pole mounting kit HDMI‑to‑DVI cable

GlideRite® DLT Stylet

Note: For ET tubes 6.0mm orlarger

Operations & Maintenance Manual: Introduction

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

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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

Smart Cable

Video baton

Camera and light

Single‑use Stat

Figure 5. GlideScope Direct Intubation Trainer

Video cable (Shortened for illustration)

Connector (Attaches to the monitor)

Lifter blade

Video cable

Handle

Cleaning cap

Camera and light

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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 6. 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.

Operations & Maintenance Manual: Introduction

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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 7. 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

Operations & Maintenance Manual: Introduction

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SETTING UP

WARNING

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

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/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 8 or Figure 9). These solutions make it easy for

you to move the system from one location to another.

• Mount it on an IV pole (Figure 10).

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 8. Premium Cart Figure 9. Mobile Stand Figure 10. IV Pole Mount

IV pole mount

Operations & Maintenance Manual: Setting up

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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

Operations & Maintenance Manual: Setting up

Page 28

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.

Page 29

PROCEdURE 4. CHARGE THE MONITOR BATTERY

WARNING

In order to maintain electrical safety, use only the provided, medical‑approved power supply.

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 11. 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.

Operations & Maintenance Manual: Setting up

Page 30

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

Page 31

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56.

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

Page 32

PROCEdURE 7. CONNECT TO AN EXTERNAL MONITOR (OPTIONAL)

WARNING

The external monitor must be safety‑approved medical equipment.

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.

Page 33

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

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 13, 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56.

• Audio Recording

• Auto Recording

• Auto External Video

• Clinic Name

Figure 12. User Settings Screen Page 1

Figure 13. 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.

Page 34

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/support.

REQUIREd CHECKS

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

2. Attach the video cable 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 or GlideScope Direct blade.

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.

Page 35

7. Press the Record button . Recording starts.

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 StoreSM)

• 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

Page 36

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.

WARNING

GlideScope systems are delivered nonsterile and require cleaning or disinfection prior to initial use.

WARNING

Report any suspected defects to Verathon® Customer Care. For contact information, visit

verathon.com/support.

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:

• Procedure 1: Connect the Video Cable to the Monitor

• Procedure 2: Insert the Video Baton into the Stat (Single‑Use Only)

• Procedure 3: Prepare the GlideScope System

• Procedure 4: Intubate Using a Video Baton and Stat

• Procedure 5: Intubate Using the GlideScope Direct

• Procedure 6: Use the Record & Snapshot Features (Optional)

• Procedure 7: Use the Playback Feature (Optional)

Page 37

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.

Table 4. Video Laryngoscope Sizes

SIZES

Stat Video Baton Recommended Patient Weight/Size

GVL® 0 Stat Video baton 1‑2 Patients less than 1.5 kg (3.3 lbs)*

GVL 1 Stat Video baton 1‑2 Patients between 1.5–3.8 kg (3.3–8.4 lbs)* GVL 2 Stat Video baton 1‑2 Patients between 1.8–10 kg (4–22 lbs)*

GVL 2.5 Stat Video baton 1‑2 Patients between 10–28 kg (22–61.7 lbs)*

GVL 3 Stat Video baton 3‑4 Patients between 10 kg–adult (22 lbs–adult)*

GVL 4 Stat Video baton 3‑4

* Weight ranges are approximate; a medical professional must evaluate on a patient‑by‑patient basis.

1. Ensure the video laryngoscope and other system components have been properly cleaned and disinfected. For more information, see the Cleaning & Disinfecting chapter.

Patients between 40 kg–large adult

(88 lbs–large adult)*

2. Using the information in Table 4, in combination with a clinical assessment of the patient and the experience and judgment of the clinician, select the single‑use 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

Page 38

PROCEdURE 2. INSERT THE VIdEO BATON INTO THE STAT (SINGLE‑USE ONLY)

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.

Page 39

PROCEdURE 4. INTUBATE USING A VIdEO BATON ANd STAT

If you are using a GlideScope Direct intubation trainer, skip to the next procedure, Intubate Using the

GlideScope Direct.

WARNING

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

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.

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

Page 40

PROCEdURE 5. INTUBATE USING THE GLIdESCOPE dIRECT

WARNING

Report any suspected defects to Verathon® Customer Care. For contact information, visit

verathon.com/support.

The following techniques are recommended for use of the GlideScope Direct intubation trainer. Ensure that the GlideScope Direct has been properly cleaned and high‑level disinfected prior to use.

OptiOn 1. RiGHt‑SiDED AppROACH

This option details the use of a right‑sided approach to the mouth, pharynx, and glottis.

1. The patient is optimally positioned with either extension of the neck or a “classic snifﬁng position.”

2. The mouth is opened, and efforts are made to minimize contact with the lips and teeth. The GlideScope Direct is introduced along the right side of the tongue, which is displaced leftward.

3. The GlideScope Direct is advanced along the tongue base until the epiglottis is seen. The GlideScope Direct tip is placed in the vallecula, lifting the epiglottis by tension on the hyoepiglottic ligament.

4. A direct line‑of‑sight to the glottis may be achieved by elevation of the epiglottis. The operator can view this directly, and the instructor can observe the progress on the video monitor.

5. The use of a stylet is optional. The operator attempts to introduce the endotracheal tube through the vocal cords.

OptiOn 2. MiDLinE AppROACH

This option details the use of a midline approach to the mouth, pharynx, and glottis.

1. The patient is optimally positioned with either extension of the neck or a “classic snifﬁng position.”

2. Using the GlideScope Direct, the operator then enters the midline of the mouth, attempting to see directly to the epiglottis (guide to the glottis) and then the GlideScope Direct tip is placed in the vallecula, lifting the epiglottis by tension on the hyoepiglottic ligament.

3. The operator now attempts to gain a line‑of‑sight of the glottis, and the instructor observes the progress on the video monitor.

4. Where necessary, the operator may also observe the video view.

Page 41

PROCEdURE 6. USE THE RECORd & SNAPSHOT FEATURES (OPTIONAL)

WARNING

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

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.

Operations & Maintenance Manual: Using the Device

Page 42

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

20130411_213043.avi

20131101_132115.avi

20131101_132217.jpg

20130411_143605.avi

20140110_203355.avi

20140114_203419.avi

20140114_205213.jpg

Tutorial

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.

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 StoreSM)

• 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)

PROCEdURE 7. USE THE PLAYBACK FEATURE (OPTIONAL)

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56.

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 14. Playback Menu

Page 43

4. Navigate the menu as follows:

• 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.

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

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.

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. The GlideRite® Rigid Stylet has been designed

to complement the angle of the GlideScope video laryngoscope to facilitate intubation. For more information about the stylet, see the GlideRite Rigid Stylet Operations and Maintenance Manual.

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

Page 44

CLEANING & DISINFECTING

GENERAL INFORMATION

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

Ensure that you follow the manufacturer’s instructions for handling and disposing of the cleaning and disinfection solutions provided in this manual.

WARNING

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.

Page 45

WARNING

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

Cleaning and disinfecting the system is an important part of using and maintaining it. Prior to each use, ensure that all system components have been cleaned, disinfected, or sterilized according to the guidance provided in Table 5. You should also examine the system periodically to make sure it is operating correctly. For more information, see the Maintenance & Safety chapter on page56.

This chapter is divided into the following sections:

• General Information—Contains an overview of system information and provides the cleaning and

disinfection procedures that are common to the system

• Video Batons—Contains the cleaning and disinfection procedures for the AVL video baton

• Direct Intubation Trainer—Contains the cleaning and disinfection procedure for the GlideScope Direct

intubation trainer

Prior to cleaning or disinfecting, ensure the protective cap is properly ﬁtted on the video cable connector. The arrow on the connector plug should match to the dot on the protective cap.

Correct ﬁtting Incorrect ﬁtting

IMPORTANT

Do not let any contaminant(s) dry on the device. Bodily contaminants tend to become securely attached to solid surfaces when dried, making removal more difﬁcult.

When using any of the disinfectants listed in this manual, read and comply with product use instructions in all applications.

Operations & Maintenance Manual: Cleaning & Disinfecting

Page 46

Note: It is understood that all items in the following table will be used as intended, and the level of disinfection or sterilization required may vary according to local regulations.

Table 5. System Risk Classiﬁcation

DEVICE PACKAGED USE

SPAULDING’S/CDC

CLASSIFICATION

Smart Cable Nonsterile Reusable Noncritical X

DISINFECTION LEVEL

STERILIZE

Low High

Monitor* Nonsterile Reusable Noncritical

Cradle* Nonsterile Reusable Noncritical

Cart* Nonsterile Reusable Noncritical

GVL® Stat

Video baton

†

‡

Sterile Single‑Use Semi‑critical

Nonsterile Reusable Noncritical X

GlideScope Direct Nonsterile Reusable Semi‑critical X

GlideRite® Rigid Stylet§Nonsterile Reusable Semi‑critical X

* Clean the video monitor, cradle, and cart when they are visibly soiled and on a regular basis, as per a schedule established by the medical

care facility or provider.

† Single‑use Stats may not be cleaned, disinfected, or sterilized. Dispose of single‑use Stats after use.

‡ The video baton is a nonsterile, reusable device, which is protected from contact with mucous membranes and non‑intact skin by the

Stat (sterile, single‑use) when used as intended. Low‑level disinfection is recommended for the video baton after every patient use. High‑level disinfection is required for the video baton when it is visibly soiled.

§ For instructions on cleaning and disinfection, see the GlideRite Rigid Stylet Operations and Maintenance Manual.

|| The low‑level disinfection solutions in this manual are not available in all geographic regions. If they are not available in your region, such

as the United States, use a high‑level disinfection method only.

X Checked boxes show minimum disinfection level requirement.

Shaded areas indicate that the disinfection/sterilization level is not required or not compatible with the device materials.

Unshaded areas show permissible levels of disinfection or sterilization based on compatibility with the device materials.

Page 47

COMPATIBILITY

Table 6 shows the disinfectant and cleaning products that have demonstrated compatibility with system

materials but have not been tested for biological efﬁcacy. Solutions included in the cleaning, disinfection, and sterilization procedures have demonstrated both compatibility and biological efﬁcacy.

Results with compatible solutions may vary based on exposure periods and device handling. Ensure that you adhere to an inspection schedule as described in Periodic Inspections on page56.

Availability of cleaning and disinfection products varies by country, and Verathon is unable to test products in every market. For more information, please contact Verathon Customer Care or your local representative. For contact information, visit verathon.com/support.

Table 6. Compatible Pre‑Cleaners, Cleaning Solutions, and Disinfectants

Ecolab® MetalClean 1500 Ecolab® Enzymatic Detergent 1000 2000 1500 Ecolab® OptiPro™ Gel Instrument Pre‑Cleaner 1500 schülke® thermosept® ER cleaner 1500 Anios® Anioxyde® 1000 high level disinfectant and cold sterilant 1500 neodisher® MediClean forte 1500 Anios® Aniosyme® XL3 enzymatic detergent 1500 STERIS® PRE‑Klenz™ Instrument Transport Gel 1000 2000 1500 Certol® ProEZFoam™ 500 Getinge® Renuzyme Foam Spray 250

PRODUCT

CYCLES PER COMPONENT

AVL Video

Baton

Video

Baton 2.0

Smart Cable

After reviewing Table 5 and Table 6, complete the following procedures to clean, disinfect, or sterilize the system components:

• Clean the GlideScope Video Monitor

• Clean the Power Adapter

• Clean the Cradle

• Clean the GlideScope Premium Cart

• Remove the Stat

• Clean & Disinfect the Video Baton

• Inspect the Video Baton

• Clean the Smart Cable

• Disinfect the Smart Cable

• Sterilize the Smart Cable (Optional)

• Clean & Disinfect the GlideScope Direct

Operations & Maintenance Manual: Cleaning & Disinfecting

Page 48

PROCEdURE 1. CLEAN THE GLIdESCOPE VIdEO MONITOR

IMPORTANT

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.

Clean the video monitor when it is visibly soiled and on a regular basis, as per a schedule established by the medical care facility or provider.

1. Turn off the video monitor, and then unplug the device.

2. Using one of the following solutions, wipe the exterior of the video monitor:

• 70% isopropyl alcohol (IPA)

• Metrex® CaviWipes™

• AHP® Oxivir

• PDI® SaniCloth® AF3 Germicidal Wipes

PROCEdURE 2. CLEAN THE POWER AdAPTER

Clean the power adapter when it is visibly soiled and on a regular basis, as per a schedule established by the medical care facility or provider. 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.

PROCEdURE 3. CLEAN THE CRAdLE

Clean the cradle when it is visibly soiled and on a regular basis, as per a schedule established by the medical care facility or provider.

1. Wipe the cradle with a standard hospital‑grade, surface‑cleaning product.

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PROCEdURE 4. CLEAN THE GLIdESCOPE PREMIUM CART

Clean the cart when it is visibly soiled and on a regular basis, as per a schedule established by the medical care facility or provider.

Table 7. Cleaning Methods for the GlideScope Premium Cart*

PRIMARY ACTIVE

INGREDIENT

†

BRAND NAME CONCENTRATION

Sodium hypochlorite Clorox® Bleach 0.16% (1600ppm)

Virox® Technologies Accel® TB Wipes

Hydrogen peroxide

0.5%

Diversey® Oxivir® TB Wipes

Isopropyl alcohol — 70%

Quaternary ammonium

compound (alcohol‑based)

* All solutions have been tested for 100compatibility cycles. Exceeding the recommended number of cycles may affect the potential life of

the product.

† See solution manufacturer’s label for additional active and inactive ingredients.

PDI® Super Sani‑Cloth® Germicidal Disposable Wipes 0.5% Metrex® CaviWipes™ 0.28%

1. If you are using bleach, prepare the solution to the concentration indicated in Table 7.

Note: If you are using a product containing 5% bleach, dilute 120mL (4ounces) of bleach in 3.8L (1gallon) of water.

2. Using one of the solutions in Table 7, expose the cart to the cleaning solution according to the solution manufacturer’s instructions.

VIDEO BATONS

For more information about the risk classiﬁcation of AVL system components, see Table 5 on page38.

PROCEdURE 5. REMOVE THE STAT

The GVL® Stat is a sterile, single‑use device. After each use, it is a biohazard, and it should be removed from the video baton and disposed of in a manner consistent with local protocols.

1. Hold the Stat in one hand.

2. To reduce the force required to remove the video baton from the Stat, use your thumb and ﬁnger to gently press the collar of the Stat.

Operations & Maintenance Manual: Cleaning & Disinfecting

Page 50

3. With the other hand, grasp the handle of the video baton and pull ﬁrmly.

PROCEdURE 6. CLEAN & dISINFECT THE VIdEO BATON

When used as intended, the video baton is a nonsterile, reusable device, which is protected from contact with mucous membranes and non‑intact skin by the Stat (sterile, single‑use). Low‑level disinfection is recommended for the video baton after every patient use. High‑level disinfection is required for the video baton when it is visibly soiled.

IMPORTANT

Do not use metal or abrasive brushes, scrub pads, or rigid tools to clean the video baton. The window that protects the camera and light can be scratched, permanently damaging the device.

This component is heat‑sensitive, and exposing it to temperatures in excess of 60°C (140°F) will cause damage to the electronics.

Bleach may be used on the video baton, but pay special attention to the stainless steel on the component, as bleach can corrode stainless steel.

Table 8. Cleaning & Disinfection Methods for the GlideScope Video Baton

PRODUCT

Enzymatic debridement

agent/detergent

DISINFECTION

LEVEL

CONDITIONS

Cleaner As per chemical manufacturer’s instructions

Up to 2000 cycles as per the following instructions:

Exposure: Prepare solution in warm water at ⅛ to ½ ﬂ. oz. per gallon (1–4 mL/L). Soak component for at least 3 minutes.

STERIS® Prolystica 2x

Concentrate Enzymatic

Presoak and Cleaner

Cleaner

Before removing from solution, brush all surfaces using a soft‑bristled brush, paying special attention to hard‑to‑reach areas. Use a cotton swab for the camera window to avoid damaging the window.

Rinse: Rinse for 3 minutes under warm running water. If component is soaked for longer than 3 minutes, increase rinse time in proportion to soak time.

Bleach (500 ppm) Low As per chemical manufacturer’s instructions

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PRODUCT

Isopropyl alcohol solution

(70%)

DISINFECTION

LEVEL

CONDITIONS

Low As per chemical manufacturer’s instructions

Oxivir® Tb Wipes Low Up to 1100 cycles as per chemical manufacturer’s instructions

Sani‑Cloth® Bleach Wipes Low Up to 750 cycles as per chemical manufacturer’s instructions

Cleaner Up to 2000 cycles as per chemical manufacturer’s instructions

SaniCloth® AF3 Germicidal

Wipes

Low

Exposure: Using fresh wipe(s), wet all surfaces and allow to remain wet for 3 minutes.

Rinse: Not applicable. Allow the component to thoroughly air dry.

ASP® CIDEXPLUS® 28Day

Solution

High As per chemical manufacturer’s instructions

ASP® CIDEX® OPA High As per chemical manufacturer’s instructions

Metrex® MetriCide®

Plus30

High As per chemical manufacturer’s instructions

100 cycles in a Medivators Advantage® Plus automated endoscope reprocessor (AER) disinfection routine meeting the following requirements:

• Concentration of disinfectant – 750‑950 parts per million

• Temperature – 28°C–32°C (82.4°F – 89.6°F)

Medivators® Rapicide

High

• Exposure time – 5 minutes

• AER conﬁguration – Hookup 2‑8‑002HAN rev A

• AER parameter set – 1‑35‑101 C DISF

Sultan® Healthcare

Sporox® II

High As per chemical manufacturer’s instructions

Standard cycles in the following processors:

STERIS® S40™

or S20™

Sterilization

STERIS® SYSTEM 1® (outside U.S.) SYSTEM 1E® (in U.S.) SYSTEM 1 EXPRESS (outside U.S.) SYSTEM 1 PLUS (outside U.S.)

STERIS® V‑PRO® low

temperature sterilization

Sterilization Up to 200 cycles as per manufacturer’s instructions

systems

STERRAD® 100S (in U.S.),

ASP® Hydrogen

PeroxideGas Plasma

Sterilization

STERRAD® 100S short cycle (outside U.S.), STERRAD® NX standard cycle, or STERRAD® 100NX standard cycle

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Page 52

PREPARE THE VIdEO BATON FOR CLEANING

1. Ensure the video monitor has been turned off.

2. Detach the video cable from the monitor by turning the connector ring in the direction of the arrow.

Connector ring

3. If you are cleaning a Video Baton 2.0, skip to the section Clean the Video Baton.

4. Place the protective cleaning cap over the connector. Ensure that the mark on the cap is aligned with the arrow on the cable.

CLEAN THE VIdEO BATON

5. Wash the video baton manually using a hospital‑grade equipment detergent or an enzymatic debridement agent/detergent. For more information, see Table 8.

IMPORTANT

Be sure to remove all foreign material, such as soil and organic material, from the surface of the component.

6. Rinse the video baton in clean, running water.

The video baton can now be disinfected.

dISINFECT OR STERILIZE THE VIdEO BATON

7. Ensure the equipment is clean according to the previous steps.

8. Ensure the protective caps on the connectors are secure.

9. Prepare and condition the disinfection solution according to the solution manufacturer’s instructions and the conditions stated in Table 8.

Page 53

10. Disinfect the video baton according to the conditions stated in Table 8. The exposure process and times vary depending on the solution and the component.

IMPORTANT

If you are using pre‑moistened wipes, wipe down the component as often as needed to keep it

visibly wet throughout the speciﬁed exposure time. You may use multiple wipes if necessary.

11. If applicable, rinse the video baton according to the solution manufacturer’s instructions.

12. Dry the video baton as appropriate for the disinfectant you are using.

If you are using … Then …

A liquid disinfectant

Pre‑moistened wipes Allow the component to air dry completely.

13. Inspect the video baton according to the instructions in the following procedure, and then store the disinfected video baton in a clean environment.

Use a sterile cloth, hospital‑grade clean air, or a low‑temperature dryer to dry the component.

PROCEdURE 7. INSPECT THE VIdEO BATON

WARNING

Report any suspected defects to Verathon® Customer Care. For contact information, visit

verathon.com/support.

1. Visually inspect the video baton for signs of damage. Perform a routine inspection of the video baton before and after every use to ensure that all endoscopic components are free of unintended rough surfaces, sharp edges, protrusions, or cracks.

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Page 54

PROCEdURE 8. CLEAN THE SMART CABLE

WARNING

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.

Use this procedure in order to clean the Smart Cable. It is critical to remove all traces of contamination from the component prior to completing disinfection or sterilization procedures. The Smart Cable is IPX7 compliant and may be completely immersed in cleaning and disinfecting solutions. The use of protective caps is not required during reprocessing.

To signiﬁcantly reduce the amount of effort needed to clean the system, do not let contaminant(s) dry on any system component. Bodily contaminants tend to become securely attached to solid surfaces when dried, making removal more difﬁcult.

Verathon has validated the products in this procedure for both chemical compatibility and biological efﬁcacy when cleaning the indicated component(s) as instructed in the Conditions column.

Table 9. Cleaning Methods for Smart Cables

PRODUCT LEVEL CYCLES* CONDITIONS

Exposure: Prepare solution in warm water at ⅛ to ½ ﬂ. oz.

per gallon (1–4 mL/L). Soak component for at least 3 minutes. Before removing from solution, brush all surfaces using a

STERIS®

Prolystica® 2X

Concentrate

Cleaner 1500

soft‑bristled brush, paying special attention to hard‑to‑reach areas. Use a cotton swab for the camera window to avoid damaging the window.

Rinse: Rinse for 3 minutes under warm running water. If component is soaked for longer than 3 minutes, increase rinse time in proportion to soak time.

Water temperature: 33–40°C (91–104°F)

Exposure: Spray all surfaces until drenched. Allow to remain

wet for 10minutes. Brush all surfaces. Rinse under running water for 5minutes. Spray all surfaces until drenched. Allow to

Metrex®

CaviCide

Cleaner 1500

remain wet for 10minutes.

Rinse: Rinse under running water for 5minutes. Fully immerse in water and agitate for 3minutes. Before removing from water, brush the cable with a soft‑bristled brush. Remove from water and ﬂush the connectors with running water and a syringe. Fully immerse in fresh water and agitate for 3minutes. Rinse under running water for 2minutes.

Page 55

PRODUCT LEVEL CYCLES* CONDITIONS

Water temperature: 19–29°C (66–84°F)

Exposure: Prepare solution at 1ounce/gallon (7.8mL/L). Soak

Metrex®

EmPower

™

Cleaner 1500

component for 3minutes. Before removing from solution, brush all surfaces and pay special attention to hard‑to‑reach areas.

Rinse: Rinse for 3minutes under running water.

Tristel™ Trio

Wipes System

(outsideU.S.)

Cleaner 1500

Pre‑clean: Use 2 or more pre‑clean towelettes to remove all visible contamination from the component.

Continue to the entry "Tristel™ Trio Wipes System" in Table 10 on page50.

Water temperature: 19–29°C (66–84°F)

Exposure: Prepare solution at 1ounce/gallon (7.8mL/L) in

Pro‑Line

Solutions

EcoZyme

Cleaner 1500

30–40°C (86–104°F) water. Soak component for 5minutes. Before removing from solution, brush all surfaces and pay special attention to hard‑to‑reach areas. Using a syringe, ﬂush the connectors.

Rinse: Rinse for 5minutes under running water. Using a syringe, ﬂush the connectors.

Water temperature: N/A

Metrex®

CaviWipes™

Metrex®

CaviWipes1™

Wip’Anios

Premium

(outsideU.S.)

Clinell®

Universal

Sanitizing

Wipes

(outsideU.S.)

Cleaner 1500

Exposure: Use towelette(s) to remove all visible contamination from the component. Using fresh towelette(s), wet all surfaces and allow to remain wet for 3minutes.

Rinse: N/A. Allow the component to thoroughly air dry. Use 3 or more towelettes to remove all visible contamination

from the component.

Continue to the entry "Metrex® CaviWipes1™" in Table 10 on page50.

Water temperature: N/A

Exposure: Use towelette(s) to remove all visible contamination

from the component. Using fresh towelette(s), wet all surfaces and allow to remain wet for 5minutes.

Rinse: N/A. Allow the component to thoroughly air dry. Water temperature: N/A

Exposure: Use towelette(s) to remove all visible contamination

from the component. Using fresh towelette(s), wet all surfaces and allow to remain wet for 5minutes.

Rinse: N/A. Allow the component to thoroughly air dry.

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PRODUCT LEVEL CYCLES* CONDITIONS

Water temperature: N/A

Sani‑Cloth®

Active Wipes

Cleaner 1500

Exposure: Use towelette(s) to remove all visible contamination from the component. Using fresh towelette(s), wet all surfaces and allow to remain wet for 5minutes.

Rinse: N/A. Allow the component to thoroughly air dry.

Sani‑Cloth®

AF3 Germicidal

Cleaner 1500

Wipes

Ecolab®

OptiPro™

Multi

Enzymatic

Cleaner 1500

Low‑Foam

Detergent

* Value indicates number of compatibility cycles tested on the component. Exceeding the recommended number of cycles may affect the

potential life of the product.

Exposure: Using fresh wipe(s), wet all surfaces and allow to remain wet for 3 minutes.

Rinse: Not applicable. Allow the component to thoroughly air dry.

Exposure: Prepare working solution at a concentration of

7.0–15.6 mL per L, or 0.5–2 U.S. ﬂuid ounces per U.S. gallon.‡ Soak components for 2–5 minutes. After soaking, brush all surfaces with a soft‑bristled brush in order to remove any visible contamination.

1. Ensure the video monitor has been turned off.

2. Detach the Smart Cable from the monitor by turning the connector ring in the direction of the releasearrow.

Connector ring

3. Detach the Smart Cable from the video baton by holding the Smart Cable connector in one hand and the base of the baton in the other, and then pulling.

4. If you are using a wipe method to clean the component, skip to Step 10.

5. If you are using a pre‑cleaning solution, apply it to the component as speciﬁed in Table 10.

6. Using the water temperature speciﬁed in Table 10, rinse the component in clean tap water and scrub with a soft‑bristled brush until all visible contamination has been removed.

7. Examine the connectors on both ends of the Smart Cable for contamination.

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8. If there is any visible sign of contamination in the connectors, use a long, soft‑bristled brush or cotton swab to remove it.

9. Prepare one of the approved cleaning solutions in Table 10 according to the solution manufacturer’s instructions.

10. Expose the components to the cleaning solution according to the instructions in Table 9. The exposure process and times vary depending on the solution and the component.

Note:

• If you are using Metrex® CaviCide®, spray additional solution as needed in order to ensure that the

component remains visibly wet for the duration of the exposure period.

• If you are using a wipe method, rewipe the component as needed in order to ensure that it remains

visibly wet for the duration of the exposure period. You may use multiple wipes as necessary.

11. If applicable for the cleaning solution, rinse the components according to the instructions in Table 9. The rinsing process and times vary depending on the solution and the component.

WARNING

To reduce the risk of cytotoxic residual when cleaning with Metrex® CaviCide®, thoroughly rinse the component as instructed in this manual.

12. Visually inspect the component for contamination. If there is any sign of contamination, restart theprocedure.

13. Using hospital‑grade clean air, which is free from oils and residuals found in common compressed air, blow out the connectors. This dries the connectors and removes any remaining residuals.

14. Using a clean, lint‑free cloth, hospital‑grade clean air, or a low‑temperature dryer, dry the component.

Note: If you are using a wipe method, allow the component to thoroughly air dry.

15. Examine the component for any signs of damage. Reusable titanium blades should not have any signs of damage other than minor surface scratches or discoloration of the metal as the result of use. If damage is present, do not use the component, and contact Verathon® Customer Care.

The component should now be clean and free of contamination. Handle the product carefully to avoid recontamination.

Note: Before each use, Smart Cables must be low‑level disinfected.

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PROCEdURE 9. dISINFECT THE SMART CABLE

Before each use, Smart Cables must be low‑level disinfected. Use the following instructions to disinfect the Smart Cable. In this procedure, the term purewater refers to water that is suitable for disinfection according to local regulations and your medical facility.

When high‑level disinfecting a Smart Cable, you may use a Medivators® CER Optima1&2AER, DSD‑201AER, or SSD‑102AER system, provided you do the following:

• Use an approved high‑level disinfectant from Table 10.

• Use a disinfectant that is compatible with the Medivators® system. For more information about

chemical compatibility, contact Medivators.

• Use the conditions provided in Table 10, such as temperature, exposure, and concentration.

• Do not expose the component to temperatures exceeding 60°C (140°F) on any cycle.

Verathon has validated the products in this procedure for both chemical compatibility and biological efﬁcacy when disinfecting Smart Cables as instructed in the Conditions column.

Table 10. Disinfection Methods for Smart Cables

PRODUCT

Sani‑Cloth®

Bleach Germicidal Disposable

Wipes

Clinell®

Universal

Sanitizing Wipes

(outsideU.S.)

Clorox® Bleach

Germicidal

Wipes

Metrex®

CaviWipes1™

DISINFECTION

LEVEL

Low 1500

CYCLES* CONDITIONS

Exposure: Using a Sani‑Cloth® Bleach Wipe, wipe the

product in order to remove any heavy soil, and then using a new wipe, thoroughly wet all surfaces of the product. Allow all surfaces to remain visibly wet for a minimum of 4 minutes. Use additional wipes as needed to ensure the surfaces stay wet.

Rinse: N/A. Allow the component to thoroughly air dry. Conditioning: N/A Water temperature: N/A Exposure: Using fresh towelette(s), wet all surfaces and

allow to remain wet for 6minutes.

Rinse: N/A. Allow the component to thoroughly airdry. Conditioning: N/A Water temperature: N/A Exposure: Using fresh towelette(s), wet all surfaces and

allow to remain wet for 3minutes.

Rinse: N/A. Allow the component to thoroughly airdry. Conditioning: N/A Water temperature: N/A Exposure: Using fresh towelette(s), wet all surfaces and

allow to remain wet for 1minute.

Rinse: N/A. Allow the component to thoroughly airdry.

Page 59

PRODUCT

STERIS® S40™

orS20™

Tristel™ Trio

Wipes System

(outsideU.S.)

STERIS®

Revital‑Ox™

Resert® XLHLD

Revital‑Ox™

Resert® HLD/

Chemosterilant

Resert® XL HLD

DISINFECTION

LEVEL

High 750

High 1500

†

High 1500

†

CYCLES* CONDITIONS

Standard cycles in the following processors: STERIS® SYSTEM 1® (outside U.S.) SYSTEM 1E® (in U.S.) SYSTEM 1 EXPRESS (outside U.S.) SYSTEM 1 PLUS (outside U.S.)

Clean according to the entry "Tristel™ Trio Wipes

System" in Table 9 on page46.

Sporocidal: Apply two pumps of the activator foam to a sporocidal towelette and manipulate towelette for 15seconds. Wet all surfaces of the component and allow to remain wet for 30seconds.

Rinse: Use a rinse towelette to wipe all surfaces.

Conditioning: 20°C (68°F) or higher

Water Temperature: 20°C (68°F) or higher

Exposure: Soak for 8minutes, ensuring that all air

bubbles are removed from the surface of the component.

Rinse: (1) 1‑minute immersion with agitation in purewater. Ensure the connector is properly rinsed.

Conditioning: 20°C (68°F) or higher

ASP®

Cidex® OPA

Metrex®

MetriCide®

OPAPlus

Medivators®

Rapicide®

OPA /28

Anios/Farmec®

OPASTER

High 1500

Water Temperature: 20°C (68°F) or higher

Exposure: Soak for 10minutes, ensuring that all air

bubbles are removed from the surface of the cable.

Rinse: (3) 1‑minute immersions with agitation in purewater. Conditioning: 20°C (68°F) or higher

Water Temperature: 20°C (68°F) or higher

Exposure: Soak for 10minutes, ensuring that all air

bubbles are removed from the surface of the cable.

Rinse: (3) 1‑minute immersions with agitation in purewater. Conditioning: 20°C (68°F) or higher

Water Temperature: 20°C (68°F) or higher

Exposure: Soak for 10minutes, ensuring that all air

bubbles are removed from the surface of the blade.

Rinse: (3)1‑minute immersions with agitation in pure water Water Temperature: 20°C (68°F)

Exposure: Soak the component for 30 minutes in

OPASTER solution, ensuring that all air bubbles are removed from the surface. Use the solution at full strength.

Rinse: (3) 1‑minute immersions with agitation in pure water. Ensure that any exposed connectors are properly rinsed.

Operations & Maintenance Manual: Cleaning & Disinfecting

Page 60

PRODUCT

DISINFECTION

LEVEL

CYCLES* CONDITIONS

Concentration: 850±100parts per million

Medivators®

Conditioning: 28–32°C (82–90°F)

Rapicide® PA

30°C

High 100

Exposure: 5minutes in a Medivators® Advantage PlusAER reprocessing system with the following conﬁguration:

• Hookup: 2‑8‑002HAN Rev. B

• Parameter: 1‑24‑010CDISF

* Value indicates number of compatibility cycles tested on the component. Exceeding the recommended number of cycles may

affect the potential life of the product.

† This chemical may cause discoloration of metal components, but the discoloration does not affect system efﬁcacy or

functionality.

‡ The minimum concentration shown in metric units is higher than the minimum concentration shown in U.S. units. This is

consistent with the manufacturer’s current instructions.

1. Ensure the Smart Cable has been properly cleaned, according to the procedure Clean the Smart Cable.

2. Prepare and condition the disinfection solution according to the solution manufacturer’s instructions and the conditions stated in Table 10.

3. Disinfect the component according to the conditions stated in Table 10. The exposure process and times vary depending on the solution.

IMPORTANT

If you are using pre‑moistened wipes, wipe down the component as often as needed to keep it

visibly wet throughout the speciﬁed exposure time. You may use multiple wipes if necessary.

4. Rinse the component according to the conditions stated in Table 10. The rinsing process and times vary depending on the solution.

5. Dry the component as appropriate for the disinfectant you are using.

If you are using … Then …

A liquid disinfectant

Use a sterile cloth, hospital‑grade clean air, or a low‑temperature dryer to dry the component.

Pre‑moistened wipes Allow the component to air dry completely.

6. Examine the component for any signs of damage. If damage is present, do not use the component, and contact Verathon® Customer Care.

7. Store the component in a clean environment.

Page 61

PROCEdURE 10. STERILIZE THE SMART CABLE (OPTIONAL)

Smart Cables are considered to be noncritical devices Therefore, sterilization of the Smart Cable is optional. Your medical care facility or provider may require sterilization of this component prior to use.

Verathon has validated the products in this procedure for both chemical compatibility and biological efﬁcacy when sterilizing Smart Cables as instructed in the Conditions column.

IMPORTANT

This component is heat‑sensitive, and exposing it to temperatures in excess of 60°C (140°F) will cause damage to the electronics.

Table 11. Sterilization Methods for Smart Cables

PRODUCT

DISINFECTION

LEVEL

CYCLES

CONDITIONS

Standard cycles in the following processors:

STERIS® S40™

orS20™

High/

Sterilization

750

STERIS® SYSTEM 1® (outside U.S.) SYSTEM 1E® (in U.S.) SYSTEM 1 EXPRESS (outside U.S.) SYSTEM 1 PLUS (outside U.S.)

STERIS® Vaprox®

Sterilization 100

Non‑lumen cycle in any STERIS® Amsco® V‑PRO® low‑temperature sterilization system.

Use one of the following processors:

ASP® Hydrogen

Peroxide Gas

Plasma

Sterilization 100

STERRAD® 100S (in U.S.) STERRAD® 100S short cycle (outside U.S.) STERRAD® NX standard cycle STERRAD® 100NX standard cycle

* Value indicates number of compatibility cycles tested on the component. Exceeding the recommended number of cycles may affect the

potential life of the product.

1. Ensure that the component has been properly cleaned according to the procedure Clean the Smart

Cable.

2. Package the component according to the instructions provided by the manufacturer of the sterilization system (Example: trays, pouches, or wraps).

3. Sterilize the component according to the manufacturer’s instructions or according to the conditions stated in Table 11.

4. Examine the component for any signs of damage. Reusable titanium blades should not have any signs of damage other than minor surface scratches or discoloration of the metal as the result of use. If damage is present, do not use the component, and contact Verathon® Customer Care.

5. Store the component in a clean environment that is appropriate for sterile equipment.

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Page 62

DIRECT INTUBATION TRAINER

The GlideScope Direct intubation trainer requires high‑level disinfection prior to use. For more information about the risk classiﬁcation of AVL system components, see Table 5 on page38.

IMPORTANT

Do not use metal or abrasive brushes, scrub pads, or rigid tools to clean the blade. The window that protects the camera and light can be scratched, permanently damaging the device.

This component is heat‑sensitive, and exposing it to temperatures in excess of 60°C (140°F) will cause damage to the electronics.

PROCEdURE 11. CLEAN & dISINFECT THE GLIdESCOPE dIRECT

Table 12. Cleaning & Disinfection Methods for the GlideScope Direct

PRODUCT

Enzymatic debridement

agent/detergent

DISINFECTION

LEVEL

CONDITIONS

Cleaner As per chemical manufacturer’s instructions

ASP® Cidex® OPA * High As per chemical manufacturer’s instructions

Metrex® MetriCide®

Plus30 *

Sultan® Healthcare

Sporox® II *

High As per chemical manufacturer’s instructions

Standard cycles in the following processors:

STERIS® S40™

or S20™ *

Sterilization

STERIS® SYSTEM 1® (outside U.S.) SYSTEM 1E® (in U.S.) SYSTEM 1 EXPRESS (outside U.S.) SYSTEM 1 PLUS (outside U.S.)

STERRAD® 100S (in U.S.),

ASP® Hydrogen

Peroxide Gas Plasma

†

Sterilization

STERRAD® 100S short cycle (outside U.S.), STERRAD® NX standard cycle, or STERRAD® 100NX standard cycle

* Tested for 500 compatibility cycles. † Tested for 100 compatibility cycles.

CLEAN THE GLIdESCOPE dIRECT

1. Ensure the video monitor has been turned off.

2. Detach the video cable from the monitor by turning the connector ring in the direction of the arrow.

Connector ring

Page 63

3. Place the protective cleaning cap over the connector. Ensure that the mark on the cap is aligned with the arrow on the cable.

4. Wash the GlideScope Direct manually using a hospital‑grade equipment detergent or an enzymatic debridement agent/detergent. For more information, see Table 12.

IMPORTANT

Be sure to remove all foreign material, such as soil and organic material, from the surface of the component.

5. Rinse the GlideScope Direct in clean, running water.

The blade can now be disinfected.

dISINFECT OR STERILIZE THE GLIdESCOPE dIRECT

1. Ensure the equipment is clean according to the previous steps.

2. Ensure the protective caps on the connectors are secure.

3. Prepare and condition the disinfection solution according to the solution manufacturer’s instructions and the conditions stated in Table 12.

4. Disinfect the GlideScope Direct according to the conditions stated in Table 12. The exposure process and times vary depending on the solution and the component.

5. If applicable, rinse the blade according to the solution manufacturer’s instructions.

6. Dry the blade by using a sterile cloth, hospital‑grade clean air, or a low‑temperature dryer.

7. Store the disinfected blade in a clean environment.

INSPECT THE GLIdESCOPE dIRECT

1. Examine the blade and integrated cable for any signs of damage. The metal blade should not have any signs of damage other than minor surface scratches as the result of use. If damage is present, do not use the component, and contact Verathon® Customer Care.

Operations & Maintenance Manual: Cleaning & Disinfecting

Page 64

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/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61.

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.

Page 65

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.

WARNING

No modiﬁcation of this equipment is allowed.

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.

DEVICE DISPOSAL

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

Operations & Maintenance Manual: Maintenance & Safety

Page 66

WARRANTY

ORIGINAL FIRST YEAR TOTAL CUSTOMER CARE WARRANTY

Verathon® warrants the system against defects in material and workmanship. The limited warranty applies for one (1) year from the date of shipment from Verathon and applies only to the original purchaser of the system. The terms of this warranty are subject to the Terms and Conditions of Sale or any other contractual document between the parties.

Verathon’s policy is to honor product warranties and to perform services only on products purchased from an authorized Verathon dealer. If you purchase a Verathon product or system components from an unauthorized dealer or if the original factory serial number has been removed, defaced or altered, your Verathon warranty will be void. Purchasing Verathon products from unauthorized entities could result in receipt of product that is counterfeit, stolen, used, defective, or not intended for use in your region.

If a customer’s system requires service or repair, Verathon will, at its discretion, either repair or replace the customer’s unit and provide a loaner unit. The customer agrees to send the defective unit to Verathon (cleaned and disinfected as appropriate) upon receipt of the loaner unit, and the customer agrees to return the loaner unit within two (2) business days of receipt of the repaired unit. All exchanged parts become property of Verathon.

Each product manufactured by Verathon is warranted to be free from defects in material and workmanship under normal use and services. Verathon’s warranty does not cover defects or problems caused by the buyer’s acts (or failure to act), the acts of others, or events beyond Verathon’s reasonable control. The buyer shall be solely responsible, for any problem, failure, malfunction, defect, claim, damage, liability, or safety issue arising out of the following:

• 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. The system shall be used in accordance with the instructions contained in this 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 is prohibited and will void all warranties.

This warranty provides coverage if the instrument is rendered inoperable as a result of an accidental drop or mishandling after payment by the buyer of the current deductible as determined by Verathon. The deductible charge will be applied on each warranty request and may be applied an unlimited number of times per instrument.

Page 67

WHAT IS COVEREd?

Warranty coverage applies to the following system components:

• GlideScope Video Monitor

• GlideScope AVL Video Baton (single‑use system only)

• GlideScope Video Baton 2.0 (single‑use system only)

• GlideScope Smart Cable (single‑use system only)

• Direct Intubation Trainer

Additional reusable components purchased either singularly or as a part of a system are warranted separately. Consumable items are not covered under this warranty.

PREMIUM CUSTOMER CARE WARRANTY

You may purchase a Premium Customer CareSM warranty that extends the limited warranty. For more information, contact Verathon® Customer Care or your local representative.

DISCLAIMER OF ADDITIONAL WARRANTIES

There are no understandings, agreements, representations of warranties expressed or implied (including warranties of merchantability or ﬁtness for a particular purpose) other than those set forth in this chapter and the Terms and Conditions of Sale. The contents of this manual do not constitute a warranty.

Some states disallow certain limitations on applied warranties. The purchaser should consult state law if there is a question regarding this disclaimer. The information, descriptions, recommendations, and safety notations in this manual are based upon Verathon experience and judgment. The contents of this manual should not be considered to be all‑inclusive or to cover all contingencies.

Operations & Maintenance Manual: Warranty

Page 68

PRODUCT SPECIFICATIONS

SYSTEM SPECIFICATIONS

Table 13. AVL System Speciﬁcation

GENERAL SPECIFICATIONS

Classiﬁcation: Electrical Class II, Applied Part BF

Line voltage:

DC power supply: 12 V DC, 2.5 A max Fuse: Internal 2.5 A Hold / 5 A Trip, 15 V max

Ingress protection against water:

Expected product life:

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

Temperature: ‑20 to 45°C (‑4 to 113°F) Relative humidity: 0 to 95% Atmospheric pressure: 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).

Video monitor IP54 Video baton IPX8 Video baton 1‑2 2 years or 1000 cycles Video baton 3‑4 2 years or 1000 cycles Video Baton 2.0 Large (3‑4) 2 years or 2000 cycles Single‑use Stat 1 use or 3‑year shelf life

OPERATING AND STORAGE SPECIFICATIONS

Operating Speciﬁcations

Shipping and Storage Conditions

Page 69

COMPONENT SPECIFICATIONS

Table 14. System Component Speciﬁcations

GLIDESCOPE VIDEO MONITOR

TFT Color, VGA 640 x 480 px

Monitor: 16.3cm (6.4 in)

Height: 174 mm

Width: 223 mm

Depth: 80 mm

Weight: 1.0 kg

Weight: 0.9 kg

Arm length: 27 cm

Width: 6.2 cm

Pole width range: 6.4–33 mm

IV POLE MOUNT

PREMIUM CART

16.3cm

223mm

174mm

80mm

Wheelbase: 53.3 cm

Min. height: 101.6cm

Max. height: 132.1 cm

Weight: 8.0–8.4kg

Operations & Maintenance Manual: Product Speciﬁcations

Page 70

Wheelbase diameter: 61 cm

Min. height: 76cm

Max. height: 122 cm

MOBILE STAND

AVL VIDEO BATON 1‑2

2041 ± 50 mm

Length of ﬂexible portion of baton: 66 mm

Height at camera: 6 mm

Width at camera: 7 mm

Video cable length: 2041 ± 50 mm

Field of view: 41°

Direction of view: 0°

66 mm

6 mm

7mm

41°

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AVL VIDEO BATON 3‑4

Length of ﬂexible portion of baton: 105 mm

Height at camera: 11 mm

Width at camera: 11 mm

Video cable length: 1540 ± 50 mm

Field of view: 49°

Direction of view: 0°

105 mm

1540 ± 50 mm

11 mm

GLIDESCOPE VIDEO BATON 2.0 LARGE (3‑ 4)

Length of ﬂexible portion of baton: 105 mm

Height at camera: 11 mm

Width at camera: 11 mm

Field of view: 49°

Direction of view: 0°

105 mm

11 mm

49°

11 mm

Operations & Maintenance Manual: Product Speciﬁcations

11 mm

49°

Page 72

Blade tip to handle: 36.2 mm

Height at camera: 8.6 mm

GVL® 0 STAT

Width at camera: 11.0 mm

Blade length in front of camera: 6.5 mm

Max blade width in front of camera: 11.0 mm

Direction of View (DOV): 0°

Insertion portion (IP) Length: 42 mm

Insertion portion (IP) Width: 15 mm

Blade tip to handle: 43.5 mm

Height at camera: 8.6 mm

11.0mm

36.2 mm

8.6 mm

6.5 mm

GVL 1 STAT

Width at camera: 10.1 mm

Blade length in front of camera: 15.0 mm

Max blade width in front of camera: 12.7 mm

Direction of View (DOV): 0°

Insertion portion (IP) Length: 50 mm

Insertion portion (IP) Width: 15 mm

8.6 mm

12.7 mm

10.1 m m

43.5 mm

15.0 mm

Page 73

Blade tip to handle: 55.7 mm

Height at camera: 8.6 mm

Width at camera: 11.2 mm

GVL® 2 STAT

Blade length in front of camera: 28.0 mm

Max blade width in front of camera: 16.0 mm

Direction of View (DOV): 0°

Insertion portion (IP) Length: 62 mm

Insertion portion (IP) Width: 18 mm

Blade tip to handle: 63.4 mm

Height at camera: 9.1 mm

GVL 2.5 STAT

8.6 mm

16.0 mm

11.2 mm

55.7 mm

28.0 mm

Width at camera: 12.7 mm

Blade length in front of camera: 37.0 mm

Max blade width in front of camera: 19.7 mm

Direction of View (DOV): +2°

Insertion portion (IP) Length: 74 mm

Insertion portion (IP) Width: 22 mm

19.7 mm

12.7 mm

63.4 mm

37.0 mm

9.1 mm

Operations & Maintenance Manual: Product Speciﬁcations

Page 74

Blade tip to handle: 77 mm

Height at camera: 14 mm

Width at camera: 16 mm

GVL® 3 STAT

Blade length in front of camera: 37 mm

Max blade width in front of camera: 20 mm

Direction of View (DOV): 0°

Insertion portion (IP) Length: 89 mm

Insertion portion (IP) Width: 25 mm

20 mm

16 mm

77 mm

14 mm

37 mm

Page 75

Blade tip to handle: 92 mm

Height at camera: 14 mm

Width at camera: 20 mm

Blade length in front of camera: 52 mm

GVL 4 STAT

Max blade width in front of camera: 27 mm

Direction of View (DOV): 0°

Insertion portion (IP) Length: 105

Insertion portion (IP) Width: 30

GLIDESCOPE DIRECT INTUBATION TRAINER

14 mm

27 mm

20 mm

92 mm

52 mm

Cable length: 1942 ± 100 mm

Height at camera: 15 mm

Width at camera: 23 mm

Blade tip to handle: 119mm

Max blade width in front of camera: 23 mm

Operations & Maintenance Manual: Product Speciﬁcations

Page 76

BATTERY SPECIFICATIONS

Table 15. 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

Page 77

ELECTROMAGNETIC COMPATIBILITY

The system is designed to be in compliance with IEC60601‑1‑2:2007, 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 16. 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

Harmonic emissions IEC61000‑3‑2

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

Group 1

Class A

Complies

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.

ELECTROMAGNETIC IMMUNITY

Table 17. 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

Operations & Maintenance Manual: Product Speciﬁcations

± 6 kV contact

± 8 kV air

± 2 kV for power supply lines

± 1 kV for input/output lines

COMPLIANCE

LEVEL

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 commercial or hospital environment.

Page 78

Table 17. 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

Surge

IEC61000‑4‑5

± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

<5% Ut (>95% dip in Ut)

for 0.5 cycle Voltage dips, short interruptions and voltage variations on power supply input lines

IEC61000‑4‑11

40% Ut (60% dip in Ut)

for 5 cycles

70% Ut (30% dip in Ut)

for 25 cycles

<5% Ut (>95% dip in Ut)

for 5 s

Power frequency (50/60Hz) magnetic ﬁeld

3 A/m In compliance

IEC61000‑4‑8

Conducted RF

IEC61000‑4‑6

3 Vrms

150 kHz to 80 MHz

COMPLIANCE

LEVEL

In compliance

3 V

ELECTROMAGNETIC ENVIRONMENT

– GUIDANCE

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

Mains power quality should be that of a typical commercial or 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 commercial or 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)

d=1.2 √P

Page 79

Table 17. 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

IEC61000‑4‑3

3 V/m

80 MHz to 2.5 GHz

COMPLIANCE

LEVEL

3 V/m

ELECTROMAGNETIC ENVIRONMENT

– GUIDANCE

d=1.2 √P 80 MHz to 800 MHz

d=2.3 √P 800 MHz to 2.5 GHz

where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m).

Field strengths from ﬁxed RF transmitters, as determined by an electromagnetic site survey,a should be less than the compliance level in each frequency range.

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

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

At 80 MHz and 800 MHz, the higher frequency range applies.

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

a. Field strengths from ﬁxed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,

AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to ﬁxed RF transmitters, an electromagnetic site survey should be considered. If the measured ﬁeld strength in the location in which the system is used exceeds the applicable RF compliance level above, the system should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re‑orienting or relocating the system.

b. Over the frequency range 150 kHz to 80 MHz, ﬁeld strengths should be less than 3 V/m.

Operations & Maintenance Manual: Product Speciﬁcations

Page 80

RECOMMENDED SEPARATION DISTANCES

Table 18 . Recommended Separation Distances between Portable and Mobile RF Communications

Equipment and the System

The system is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the system can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the system as recommended below, according to the maximum output power of the communications equipment.

RATED MAXIMUM

OUTPUT POWER OF

TRANSMITTER (W)

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73 1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

Note: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

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

SEPARATION DISTANCE ACCORDING TO FREQUENCY OF TRANSMITTER (m)

150 kHz to 80 MHz

d=1.2 √P

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.

80 MHz to 800 MHz

d=1.2 √P

800 MHz to 2.5 GHz

d=2.3 √P

Table 19. EMC Standards for Accessories

ACCESSORY LENGTH

AC power cord 4.5 m (15 ft) DC medical power adapter — HDMI‑to‑DVI cable 6 m (20 ft)

Page 81

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 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

Page 82

TERM DEFINITION

OSHA Occupational Safety and Health Administration (federal agency in U.S.) oz Ounce ppm Parts per million

Purewater

Water that is suitable for high‑level disinfection according to local regulations

and your medical facility RF Radio frequency RH Relative humidity V Volt Vrms Voltage root mean squared W Watt WEEE Waste electrical and electronic equipment

Page 83

Page 84

Verathon GlideScope, GlideScope System AVL Single-Use Operation & Maintenance Manual

Specifications and Main Features

Frequently Asked Questions

User Manual

IMPORTANT INFORMATION

PRODUCT INFORMATION

STATEMENT OF INTENDED USE

ESSENTIAL PERFORMANCE

STATEMENT OF PRESCRIPTION

NOTICE TO ALL USERS

PRECAUTIONS & WARNINGS

PRODUCT DESCRIPTION

INTRODUCTION

SYSTEM PARTS & ACCESSORIES

LANGUAGE SETTINGS

VIDEO LARYNGOSCOPE COMPONENTS

BUTTONS, ICONS, & CONNECTIONS

SETTING UP

PROCEdURE 1. PERFORM INITIAL INSPECTION

PROCEdURE 2. MOUNT THE GLIdESCOPE VIdEO MONITOR (OPTIONAL)

PROCEdURE 3. ATTACH THE VIdEO BATON CRAdLE (OPTIONAL)

PROCEdURE 4. CHARGE THE MONITOR BATTERY

PROCEdURE 5. CONNECT THE VIdEO CABLE OR SMART CABLE TO THE MONITOR

PROCEdURE 7. CONNECT TO AN EXTERNAL MONITOR (OPTIONAL)

PROCEdURE 8. CONFIGURE USER SETTINGS

PROCEdURE 9. PERFORM A FUNCTIONAL CHECK

USING THE DEVICE

PROCEdURE 1. CONNECT THE VIdEO CABLE TO THE MONITOR

PROCEdURE 2. INSERT THE VIdEO BATON INTO THE STAT (SINGLE‑USE ONLY)

PROCEdURE 3. PREPARE THE GLIdESCOPE SYSTEM

PROCEdURE 4. INTUBATE USING A VIdEO BATON ANd STAT

PROCEdURE 5. INTUBATE USING THE GLIdESCOPE dIRECT

PROCEdURE 6. USE THE RECORd & SNAPSHOT FEATURES (OPTIONAL)

PROCEdURE 7. USE THE PLAYBACK FEATURE (OPTIONAL)

CLEANING & DISINFECTING

GENERAL INFORMATION

PROCEdURE 1. CLEAN THE GLIdESCOPE VIdEO MONITOR

PROCEdURE 2. CLEAN THE POWER AdAPTER

PROCEdURE 3. CLEAN THE CRAdLE

PROCEdURE 4. CLEAN THE GLIdESCOPE PREMIUM CART

VIDEO BATONS

PROCEdURE 5. REMOVE THE STAT

PROCEdURE 6. CLEAN & dISINFECT THE VIdEO BATON

PROCEdURE 7. INSPECT THE VIdEO BATON

PROCEdURE 8. CLEAN THE SMART CABLE

PROCEdURE 9. dISINFECT THE SMART CABLE

PROCEdURE 10. STERILIZE THE SMART CABLE (OPTIONAL)

DIRECT INTUBATION TRAINER

PROCEdURE 11. CLEAN & dISINFECT THE GLIdESCOPE dIRECT

MAINTENANCE & SAFETY

PERIODIC INSPECTIONS

GLIDESCOPE VIDEO MONITOR BATTERY

SYSTEM SOFTWARE

DEVICE REPAIR

DEVICE DISPOSAL

WARRANTY

PRODUCT SPECIFICATIONS

SYSTEM SPECIFICATIONS

COMPONENT SPECIFICATIONS

BATTERY SPECIFICATIONS

ELECTROMAGNETIC COMPATIBILITY

GLOSSARY