Verathon Glidescope Ranger

GLIDESCOPE SYSTEM
RANGER SINGLE USE
Operations & Maintenance Manual
0900‑1307‑16‑60
GLIDESCOPE SYSTEM
RANGER SINGLE USE
Operations & Maintenance Manual
Effective: April 1, 2016
Caution: Federal (United States) law restricts this

device to sale by or on the order of a physician.
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.
800.331.2313 (US and Canada only)
Tel: 425.867.1348
Fax: 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: 604.439.3009
Fax: 604.439.3039
0413
Copyright © 2009, 2016 by Verathon Inc. All rights reserved.
GlideScope, the GlideScope symbol, GlideRite, GVL, 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.
TABLE OF CONTENTS
IMPORTANT INFORMATION..................................................................................................................................1
Product Description.............................................................................................................................................1
Statement of Intended Use...................................................................................................................................1
Essential Performance..........................................................................................................................................1
Statement of Prescription.....................................................................................................................................1
Notice to All Users...............................................................................................................................................1
Precautions & Warnings.......................................................................................................................................2
INTRODUCTION.....................................................................................................................................................7
Single‑Use System................................................................................................................................................7
System Parts & Accessories..................................................................................................................................8
Monitor Controls & Connections .........................................................................................................................9
Video Laryngoscope Components........................................................................................................................9
SETTING UP..........................................................................................................................................................10
Procedure 1. Perform Initial Inspection...................................................................................................... 10
Procedure 2. Charge the Monitor.............................................................................................................. 11
Procedure 3. Connect a Video Baton......................................................................................................... 13
Procedure 4. Perform a Functional Check.................................................................................................. 14
USING THE DEVICE.............................................................................................................................................. 15
Procedure 1. Connect a Video Baton......................................................................................................... 16
Procedure 2. Insert the Video Baton into the Stat...................................................................................... 17
Procedure 3. Prepare the System............................................................................................................... 18
Procedure 4. Intubate Using the GlideScope 4‑Step Technique................................................................... 19
i
Operations & Maintenance Manual: Table of Contents
CLEANING & DISINFECTING................................................................................................................................20
General Information...........................................................................................................................................20
Procedure 1. Clean the Video Monitor.......................................................................................................22
Procedure 2. Clean the Video Baton Cradle...............................................................................................22
Procedure 3. Clean the Storage Case.........................................................................................................22
Video Baton.......................................................................................................................................................23
Procedure 1. Remove the Stat...................................................................................................................23
Procedure 2. Clean & Disinfect the Video Baton........................................................................................ 24
Procedure 3. Inspect the Video Baton........................................................................................................26
MAINTENANCE & SAFETY...................................................................................................................................27
Periodic Inspections...........................................................................................................................................27
System Software................................................................................................................................................27
GlideScope Ranger Battery.................................................................................................................................27
Device Repair.....................................................................................................................................................28
Device Disposal..................................................................................................................................................28
WARRANTY.........................................................................................................................................................29
PRODUCT SPECIFICATIONS..................................................................................................................................31
System Specifications......................................................................................................................................... 31
Component Specifications.................................................................................................................................32
Electromagnetic Compatibility............................................................................................................................37
SYMBOL DIRECTORY........................................................................................................................................... 41
GLOSSARY............................................................................................................................................................43
ii
IMPORTANT INFORMATION
PRODUCT DESCRIPTION
GlideScope Ranger is a portable, compact video laryngoscope that provides a clear, real‑time view
of a patient’s airway, enabling quick intubation. The Ranger system is designed for field (military and
pre‑hospital) use.
Designed for “1st Pass Success” in military and emergency settings, the Ranger system features rugged,
high‑impact construction, patented blade angulation, a patented anti‑fogging mechanism, and a non‑glare
monitor that is easily visible in bright light. The device is dependable in an array of field conditions, making
it ideal for pre‑hospital and critical care situations. The GlideScope Ranger video laryngoscope has been
granted Airworthiness Certification from the United States Army.
The Ranger is operational in seconds. It is compact for easy carrying and storage. The integrated,
rechargeable lithium battery provides a minimum 90‑minute continuous‑use autonomy and allows for
approximately 20 intubations per battery cycle (depending on usage).
STATEMENT OF INTENDED USE

GlideScope Ranger video laryngoscopes are intended for use by qualified medical professionals to obtain a
clear, unobstructed view of the 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 Ranger 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, 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
1
Operations & Maintenance Manual: Important Information
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 37.
To maintain electromagnetic interference (EMI) within certified limits, the GlideScope Ranger
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.
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.
2
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
components will cause permanent device damage and void the warranty. For a list of approved
cleaning procedures and products, refer to the Cleaning & Disinfecting chapter.
CAUTION
The system contains electronics that could be damaged by ultrasonic and automated washing
equipment. Do not use an ultrasonic device or automated washing equipment to clean this
product.
CAUTION
The GlideScope Ranger video monitor is manufactured to be IP68 compliant. If the monitor
is disassembled during a service procedure, after reassembly, the monitor will not be IP68
compliant.
3
WARNINGS
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. For more information,
visit www.osha.gov.
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
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
Do not place the video baton in the cradle if any of the components are contaminated.
4
WARNING
Availability of cleaning, disinfection, and sterlilization 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 or disposing of the cleaning,
disinfection, or sterilization solutions provided in this manual.
WARNING
Do not reuse, reprocess or resterilize single‑use components. Reuse, reprocessing or resterilization

may create a risk of contamination of the device, cause patient infection or cross‑infection.
WARNING
This instrument and related devices may contain batteries and other environmentally hazardous
materials. When the instrument or accessories have reached the end of their useful service life,
see the section Device Disposal on page 28. Dispose of used, single‑use components as
infectious waste.
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.
5
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 to the tonsils or soft palate.
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
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.
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, causing patient infection or
cross‑infection.
6
INTRODUCTION
SINGLE‑USE SYSTEM
The GlideScope Ranger system is available in a single‑use configuration. It features a video monitor, a
reusable video baton, the cables and adapters to power the device, and any optional system components
that may facilitate intubations or provide convenience.
The laryngoscope is a reusable video baton that is inserted into a single‑use, disposable Stat. The video baton
connects to the video monitor and contains the camera and electronics that process the video data captured
by the baton. Stats are available in a wide range of sizes, and each size corresponds to one of two video
baton sizes.
Figure 1. Ranger Single‑Use System
7
Operations & Maintenance Manual: Introduction
SYSTEM PARTS & ACCESSORIES
Table 1. Required System Components
REQUIRED PARTS & ACCESSORIES
Video monitor Power supply Power cable
Video baton 1‑2 Video baton 3‑4
GVL Stat 0 GVL Stat 1 GVL Stat 2 GVL Stat 2.5 GVL Stat 3 GVL Stat 4
Table 2. Optional System Components

OPTIONAL PARTS & ACCESSORIES
GlideRite Rigid Stylet
®
Ranger Transport Bag Video Baton Cradle & Case
8
MONITOR CONTROLS & CONNECTIONS
The digital, full‑color video monitor displays the images transmitted from the camera in the video baton.
The monitor includes the screen and controls you use to operate the system. It contains a lithium battery
that provides power to the system. The system must be operated exclusively on battery power, without a
connection to an AC power source.
Figure 2. Ranger Video Monitor
Video cable connector DC power socket

(inside cradle)
Battery charge status LED

Power switch
VIDEO LARYNGOSCOPE COMPONENTS

Figure 3. Single‑Use Video Laryngoscope Components
Video baton Video cable

Single‑use Stat
Camera and light
9
Operations & Maintenance Manual: Introduction
SETTING UP
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:
• Procedure 1: Perform Initial Inspection
• Procedure 2: Charge the Monitor
• Procedure 3: Connect a Video Baton
• Procedure 4: Perform a Functional Check
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.
10
Procedure 2. CHARGE THE MONITOR
WARNING
In order to maintain electrical safety, use only the provided, medical‑approved power supply.
The video monitor includes an internal lithium battery. You must charge the battery fully prior to first use.
The system must be operated exclusively on battery power, without a connection to an AC power source.
Under normal operating conditions, a fully charged battery lasts approximately 90 minutes. For optimal
battery life, ensure that the battery is fully charged before you use the monitor.
Note: The system will not operate while charging. If you switch the instrument on during charging, the
charging light flashes.
Figure 4. Battery Charge Level Icons
Steady green—The battery is fully charged.
Flashing green—Battery power is low. The LED flashes for approximately 5 minutes before the
system turns off.
No LED—The battery is completely depleted and needs to be recharged.
Steady orange—The monitor is connected to an AC power source and the battery is charging.
Flashing orange—There is an issue with the battery.

If you observe the flashing orange light, ensure the monitor power switch is in the off position,
check the cable connections, and then disconnect and reconnect the charging cable to the monitor.
If this does not resolve the issue, contact Verathon® Customer Care.
1. Ensure that the power switch is in the OFF position.
2. Connect the video monitor 12V DC power supply to the power cord.
11
Operations & Maintenance Manual: Setting Up
3. On the front of the monitor, unscrew the power socket cap, and then connect the charging cable to the
power socket.
4. Plug the power cord into an AC power outlet.

Note: Plug varies by region.
5. Allow the battery to charge. Fully charging the battery may take up to 5 hours.
• While the battery is charging, the LED is orange.
• When the battery has completed charging, the LED turns green.
12
Procedure 3. CONNECT A VIDEO BATON
The video baton attaches directly to the video monitor, supplying power to the video baton and transmitting
video data from the camera to the monitor.
When you are ready to intubate the patient, ensure that you also complete the procedure Insert the Video
Baton into the Stat on page 17. It is recommended that you leave the single‑use Stat in the packaging
while inserting the video baton and that you do not remove the Stat from the packaging until you are ready
to perform an intubation procedure. This helps ensure that the equipment remains as clean as possible.
2. Align the dot on the video cable connector and the arrow on the video cable port.
3. Insert the video cable connector into the port. You will hear a click when the cable is
successfully connected.
4. To disconnect the video cable from the monitor, rotate the connector ring in the direction of the release
arrow, and then remove the connector from the port.
5. Continue to the procedure Perform a Functional Check on page 14.
13
Operations & Maintenance Manual: Setting Up
Procedure 4. 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 Customer Care if your system does not function as described below.
1. Ensure that you have fully charged the battery according to the instructions in Charge the Monitor on
page 11.
2. Ensure that you have attached the video baton to the monitor, according to the instructions in Connect a
Video Baton on page 13.
3. On the video monitor, turn the power switch to the ON position.
4. Look at the monitor screen, and verify that the image displayed is being received from the video baton.
14
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
initial use.
WARNING
Ranger video batons are equipped with the an 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 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 a Video Baton
• Procedure 2: Insert the Video Baton into the Stat
• Procedure 3: Prepare the System
• Procedure 4: Intubate Using the GlideScope 4‑Step Technique
15
Operations & Maintenance Manual: Using the Device
Procedure 1. CONNECT A VIDEO BATON
Table 3. 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)
Patients between 40 kg–morbidly obese
GVL 4 Stat Video baton 3‑4
(88 lbs–morbidly obese)
* Weight ranges are approximate; a medical professional must evaluate on a patient‑by‑patient basis.
1. Ensure that the battery is sufficiently charged. For more information, see Charge the Monitor on
page 11.
2. Ensure the GlideScope system components have been properly cleaned and disinfected. For more
information, see the Cleaning & Disinfecting chapter on page 20.
3. Using the information in Table 3, in combination with a clinical assessment of the patient and the
experience and judgment of the clinician, select the GlideScope video laryngoscope that is appropriate
for the patient.
5. Align the dot on the video cable connector and the arrow on the video cable port.
16
6. Insert the video cable connector into the port. You will hear a click when the cable is successfully
connected.
7. Continue to the procedure Insert the Video Baton into the Stat.
Procedure 2. INSERT THE VIDEO BATON INTO THE STAT
1. Open the GVL® Stat pouch, but do not remove the Stat from the packaging.
2. Ensure that the logo on the side of the baton and the logo on the side of the Stat are aligned.
3. Slide the video baton into the GVL Stat until it clicks into place. Do not remove the Stat from the pouch
until you are ready to begin the intubation. This ensures that the Stat remains as clean as possible.
Note: Ensure that you do not insert the video baton backwards.
Correct Incorrect
4. If needed, allow the 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 baton or Stat is
stored in cold conditions, additional warming time may be required for optimal performance of the
anti‑fog feature.
5. 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.
6. Continue to the procedure Prepare the System.
17
Procedure 3. PREPARE THE SYSTEM
1. On the video monitor, turn the power switch to the ON position.
2. On the monitor screen, verify that the image displayed is from the video baton camera.
3. If needed, allow the anti‑fog feature to warm up for 30–120 seconds, and then continue to the
procedure Intubate Using the GlideScope 4‑Step Technique on page 19.
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 baton or Stat is
stored in cold conditions, additional warming time may be required for optimal performance of the
anti‑fog feature.
18
Procedure 4. INTUBATE USING THE GLIDESCOPE 4‑STEP TECHNIQUE
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 to the tonsils or soft palate.
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.
To perform an intubation, Verathon® recommends using the GlideScope 4‑Step Technique as outlined in
this procedure. Each step begins with where the user should be looking to complete that action. Prior to
beginning this procedure, verify that the monitor is receiving an accurate image from the video laryngoscope.
1. Look in the Mouth: With the video laryngoscope in your left hand, introduce it into the midline of the
oral pharynx.
2. Look at the Screen: Identify the epiglottis, and then manipulate the blade in order to obtain the best
glottic view.
Figure 5. Ideal Glottic View
3. Look in the Mouth: Carefully guide the distal tip of the tube into position near the tip of
the laryngoscope.
4. Look at the Screen: Complete the intubation, gently rotating or angling the tube as needed to
redirect it.
19
CLEANING & DISINFECTING
GENERAL INFORMATION
WARNING
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. For more information,
visit www.osha.gov.
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
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.
For contact information, visit verathon.com/support.
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.
20
Cleaning and disinfecting the GlideScope Ranger system is an important part of using and maintaining the
system. Prior to each use, ensure that each system component has been cleaned and disinfected according to
the guidance provided in Table 4.
The following table describes the risk assessment for each system component, including the Spaulding’s/CDC
classification for the minimum required disinfection level.
Table 4. GlideScope Ranger System Risk Assessment
SPAULDING’S/CDC DISINFECTION LEVEL

DEVICE PACKAGED USE STERILIZE
CLASSIFICATION
Low High
GlideRite® Rigid Stylet§ Nonsterile Reusable Semi‑critical X
Video baton* Nonsterile Reusable Noncritical X
Video monitor †
Nonsterile Reusable Noncritical
Single‑use Stat ‡
Sterile Single‑Use Semi‑critical
Cradle† Nonsterile Reusable Noncritical
Storage case† Nonsterile Reusable Noncritical
X Checked boxes show minimum disinfection level requirement.
Shaded areas indicate that the disinfection or sterilization level is not required or not compatible with the device materials.
Unshaded areas show permissible levels of disinfection or sterilization based on compatibility with the device materials.
* When used as intended, the video baton is a nonsterile, reusable device that is protected from contact with mucous membranes and
nonintact skin by the sterile, single‑use Stat. Low‑level disinfection is required for the video baton after every patient use. High‑level
disinfection is required for the video baton when it is visibly soiled.
† Clean these components when 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.
§ For instructions on cleaning and disinfection, see the GlideRite Rigid Stylet Operations and Maintenance Manual.
After reviewing Table 4, complete the following procedures to clean, disinfect, or sterilize the
system components:
• General Information
○○ Procedure 1: Clean the Video Monitor
○○ Procedure 2: Clean the Video Baton Cradle
○○ Procedure 3: Clean the Storage Case
• Video Baton
○○ Procedure 1: Remove the Stat
○○ Procedure 2: Clean & Disinfect the Video Baton
○○ Procedure 3: Inspect the Video Baton
21
Operations & Maintenance Manual: Cleaning & Disinfecting
Procedure 1. CLEAN THE 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 Ranger video monitor, and then unplug the system from direct power.
2. Using 70% isopropyl alcohol (IPA), 100 ppm bleach solution, or a mild detergent with water, wipe the
exterior of the video monitor.
Procedure 2. CLEAN THE VIDEO BATON CRADLE
1. Using a standard, hospital‑grade surface‑cleaning product, wipe the cradle.
Procedure 3. CLEAN THE STORAGE CASE
1. Using 70% IPA, 100 ppm bleach solution, or a mild detergent and water, wipe the exterior of the case.
22
VIDEO BATON
For more information about the risk assessment of Ranger system components, see Table 4 on page 21.
Procedure 1. 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.
3. With the other hand, grasp the handle of the video baton and pull firmly.
23
Procedure 2. CLEAN & DISINFECT THE VIDEO BATON
When used as intended, the video baton is a nonsterile, reusable device that 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 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 product is heat‑sensitive, and exposing the components to temperatures in excess of 60°C (140°F)
will cause damage to the electronics and void the device warranty.
Table 5. Cleaning & Disinfection Methods for the GlideScope Ranger Video Baton
MAXIMUM
CHEMICAL DISINFECTION LEVEL
CONCENTRATION
Enzymatic debridement agent or detergent — Cleaner
Bleach* 500 ppm Low
Isopropyl alcohol solution 70% Low
Hydrogen peroxide ≤ 7.5% High
Glutaraldehyde ≤ 3.4% High
Ortho‑phthalaldehyde 0.55% High
Peracetic acid 0.2% High/Sterilization
Vaporized hydrogen peroxide† 90% Sterilization
* Bleach may be used on the video batons, but pay special attention to stainless steel components, as bleach can corrode
stainless steel.
† GlideScope Ranger video batons designed to withstand vaporized hydrogen peroxide are identified by a metal label. If the
component does not feature a metal label, do not use this solution.
CLEAN THE VIDEO BATON
1. Ensure the video monitor has been turned off.
2. Disconnect the video cable from the monitor by rotating the connector ring in the direction of the
release arrow, and then removing the connector from the port.
24
3. Place the protective cleaning cap over the connector.
4. Wash the component manually using a hospital‑grade equipment detergent or an enzymatic

debridement agent, according to the chemical manufacturer’s instructions.
5. Using warm water, rinse the component in clean tap water and scrub with a soft‑bristled brush until all
visible contamination has been removed.
To prevent damage, use a cotton swab in order to clean around the camera window.
6. Ensure all foreign material (e.g., soil and organic material) is removed from the surface of the device. It
is critical to remove all traces of contamination from the component prior to completing disinfection or
sterilization procedures.
7. Using a clean, lint‑free cloth, hospital‑grade clean air, or a low‑temperature dryer, dry the component.
The component may now be disinfected or sterilized.
DISINFECT OR STERILIZE THE VIDEO BATON
8. Ensure the equipment is clean according to the previous steps.
9. Ensure the protective cap on the connector is secure.
10. Prepare and condition the disinfection or sterilization solution according to the solution manufacturer’s
instructions and the maximum concentration stated in Table 5.
11. Disinfect or sterilize the video baton according to the solution manufacturer’s instructions. The exposure
process and times vary depending on the solution.
12. If applicable, rinse the component according to the solution manufacturer’s instructions.
13. Dry the component by using a sterile cloth, hospital‑grade clean air, or a low‑temperature dryer.
14. Inspect the video baton according to the instructions in the following procedure, and then store the
component in a clean environment.
25
Procedure 3. INSPECT THE VIDEO BATON
WARNING
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.
26
MAINTENANCE & SAFETY
PERIODIC INSPECTIONS
Periodic inspections should be performed to ensure safe and effective operation, in addition to performing
routine inspection by the user before and after every use. 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. For contact information, see
SYSTEM SOFTWARE
This manual documents the most current version of the software. If your system 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/or void the warranty.
GLIDESCOPE RANGER BATTERY

For battery specifications, see the Battery Specifications section on page 32.
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.
27
Operations & Maintenance Manual: Maintenance & Safety
DEVICE REPAIR
The GlideScope Ranger 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.
CAUTION
The GlideScope Ranger video monitor is manufactured to be IP68 compliant. If the monitor
is disassembled during a service procedure, after reassembly, the monitor will not be IP68
compliant.
DEVICE DISPOSAL
The GlideScope Ranger instrument and related devices may contain batteries and other environmentally
hazardous materials. When the instrument has reached the end of its useful service life, it must be disposed
of in accordance with WEEE requirements. Coordinate disposal through your Verathon Service Center, or
alternatively, follow your local protocols for hazardous waste disposal.
28
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.
29
Operations & Maintenance Manual: Warranty
WHAT IS COVERED?
Warranty coverage applies to the following system components:
• GlideScope Ranger video monitor
• GlideScope Ranger video baton
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.
30
PRODUCT SPECIFICATIONS
SYSTEM SPECIFICATIONS
GENERAL SPECIFICATIONS
Classification: Electrical Class II, Applied Part BF
Line voltage: 100–240 VAC, 50 and 60 Hz
DC power supply: Max 0.25 A
Ingress protection: IP68, up to 1 m (3 ft) for 60 minutes
OPERATING & STORAGE SPECIFICATIONS
Operating Specifications
Temperature: 10 to 40°C (50 to 104°F)
Relative humidity: 0–95%
Atmospheric pressure: 440–1060 hPa
Shipping and Storage Conditions
Temperature: ‑20 to 45°C (‑4 to 113°F)
Relative humidity: 0–95%
Atmospheric pressure: 440–1060 hPa
31
Operations & Maintenance Manual: Product Specifications
COMPONENT SPECIFICATIONS
VIDEO MONITOR
SPECIFICATIONS COMPONENT
Ranger Video Monitor
176 mm
LCD TFT, 320 x 240 px m

m
89
Monitor: 89 mm (3.5 in)
166 mm
Height: 166 mm
Width: 176 mm
Depth: 53 mm
Weight: 570 g
53 mm
BATTERY SPECIFICATIONS
CONDITION SPECIFICATION
Battery type Lithium
Under normal operating conditions, a fully charged battery lasts approximately
Battery life
90 minutes.
Charging time takes no more than 5 hours from an empty battery to a full
Charging time
charge.
Rated capacity 1150–1300 mAh
Nominal voltage 11.1 V
Max charging voltage 12.0‑13.2 V
32
VIDEO BATONS & STATS
Ranger Video Baton 1–2
968 mm
Cable length: 968 mm

Length of flexible baton: 66 mm
Height at camera: 6 mm
Width at camera: 7 mm
66 mm
6 mm
7 mm
Ranger Video Baton 3–4
959 mm
Cable length: 959 mm

Length of flexible baton: 106 mm
106 mm
11 mm
11 mm
33
GVL 0 Stat
Blade tip to handle: 36.2 mm
Height at camera: 8.6 mm 11.0 mm
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
36.2 mm
8.6 mm
6.5 mm
GVL 1 Stat
Height at camera: 8.6 mm
12.7 mm
Blade length in front of camera: 15.0 mm 10.1 mm
43.5 mm
8.6 mm
15.0 mm
34
GVL 2 Stat
Height at camera: 8.6 mm
16.0 mm
Blade length in front of camera: 28.0 mm 11.2 mm
55.7 mm
8.6 mm 28.0 mm
GVL 2.5 Stat

Height at camera: 9.1 mm 19.7 mm

12.7 mm
Blade length in front of camera: 37.0 mm
63.4 mm
37.0 mm
9.1 mm
35
GVL 3 Stat
Blade tip to handle: 77 mm
Width at camera: 16 mm 20 mm
Blade length in front of camera: 37 mm 16 mm
Max blade width in front of camera: 20 mm
77 mm
14 mm
37 mm
GVL 4 Stat
Blade tip to handle: 92 mm
27 mm
Blade length in front of camera: 52 mm
Max blade width in front of camera: 27 mm 20 mm
92 mm
14 mm
52 mm
36
ELECTROMAGNETIC COMPATIBILITY
GlideScope Ranger 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 GlideScope Ranger 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 systemis not affected under the test conditions described in the following tables. For more information
about the essential performance of the GlideScope Ranger system, see Essential Performance on page 1.
ELECTROMAGNETIC EMISSIONS
Table 6. Guidance and Manufacturer’s Declaration—Electromagnetic Emissions
The GlideScope Ranger system is intended for use in the electromagnetic environment specified below. The
customer or the user of the GlideScope Ranger system should assure that it is used in such an environment.
EMISSIONS TEST COMPLIANCE ELECTROMAGNETIC ENVIRONMENT – GUIDANCE
The GlideScope Ranger system uses RF energy only for its internal
RF emissions
Group 1 function. Therefore, its RF emissions are very low and are not likely
CISPR 11
to cause any interference in nearby electronic equipment.
RF emissions
Class A
CISPR 11
The GlideScope Ranger system is suitable for use in all
Harmonic emissions
Class A establishments other than domestic and those directly connected
IEC 61000‑3‑2
to the public low‑voltage power supply network that supplies
Voltage fluctuations/ buildings used for domestic purposes.
flicker emissions Complies
IEC 61000‑3‑3
37
ELECTROMAGNETIC IMMUNITY
Table 7. Guidance and Manufacturer’s Declaration— Electromagnetic Immunity
COMPLIANCE ELECTROMAGNETIC ENVIRONMENT
IMMUNITY TESTS IEC 60601 TEST LEVEL
LEVEL – GUIDANCE
Floors should be wood, concrete,
Electrostatic discharge or ceramic tile. If floors are
± 6 kV contact
(ESD) In compliance covered with synthetic material,
± 8 kV air the relative humidity should be at
IEC 61000‑4‑2
least 30%.
Electrical fast Mains power quality should be
± 2 kV for power supply lines
transient/burst In compliance that of a typical commercial or
± 1 kV for input/output lines hospital environment.
IEC 61000‑4‑4
Surge ± 1 kV line(s) to line(s) Mains power quality should be
In compliance that of a typical commercial or
IEC 61000‑4‑5 ± 2 kV line(s) to earth hospital environment.
<5% Ut (>95% dip in Ut) Mains power quality should be
for 0.5 cycle that of a typical commercial or
Voltage dips, short hospital environment. If the user
interruptions and 40% Ut (60% dip in Ut) of the GlideScope Ranger system
voltage variations on for 5 cycles requires continued operation
power supply input In compliance
70% Ut (30% dip in Ut) during power mains interruptions,
lines it is recommended that the
for 25 cycles
IEC 61000‑4‑11 GlideScope Ranger system be
<5% Ut (>95% dip in Ut) powered from an uninterruptible
for 5 s power supply or a battery.
Power frequency Power frequency magnetic fields
(50/60 Hz) magnetic should be at levels characteristic
field 3 A/m In compliance of a typical location in a
typical commercial or hospital
IEC 61000‑4‑8 environment.
Portable and mobile RF
communications equipment
should be used no closer to any
part of the GlideScope Ranger
system, including cables, than the
Conducted RF recommended separation distance
3 Vrms
3 V calculated from the equation
IEC 61000‑4‑6 150 kHz to 80 MHz
applicable to the frequency of the
transmitter.
Recommended separation
distance d (m)
d=1.2 √P
38
Table 7. Guidance and Manufacturer’s Declaration— Electromagnetic Immunity
COMPLIANCE ELECTROMAGNETIC ENVIRONMENT
IMMUNITY TESTS IEC 60601 TEST LEVEL
LEVEL – 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).
Radiated RF Field strengths from fixed RF

3 V/m
3 V/m transmitters, as determined
IEC 61000‑4‑3 80 MHz to 2.5 GHz
by an electromagnetic site
survey,a should be less than
the compliance level in each
frequency range.b
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 GlideScope Ranger system is used exceeds the applicable RF compliance level above, the GlideScope Ranger 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 GlideScope Ranger system.
b. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
39
RECOMMENDED SEPARATION DISTANCES
Table 8. Recommended Separation Distances between Portable and Mobile RF Communications
Equipment and the GlideScope Ranger System
The GlideScope Ranger system is intended for use in an electromagnetic environment in which radiated
RF disturbances are controlled. The customer or the user of the GlideScope Ranger system can help
prevent electromagnetic interference by maintaining a minimum distance between portable and mobile
RF communications equipment (transmitters) and the GlideScope Ranger system as recommended below,
according to the maximum output power of the communications equipment.
RATED MAXIMUM SEPARATION DISTANCE ACCORDING TO FREQUENCY OF TRANSMITTER (m)

OUTPUT POWER OF 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
TRANSMITTER (W) d=1.2 √P d=1.2 √P d=2.3 √P
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.
ACCESSORY CONFORMANCE TO STANDARDS

To maintain electromagnetic interference (EMI) within certified limits, the system must be used with the
cables, components, and accessories specified or supplied by Verathon®. For additional information, see the
System Parts & Accessories and Component Specifications sections. The use of accessories or cables other
than those specified or supplied may result in increased emissions or decreased immunity of the system.
Table 9. EMC Standards for Accessories

ACCESSORY MAX LENGTH
AC power cord 0.6 m (3 ft)
Medical power supply —
40
SYMBOL DIRECTORY
SYMBOL MEANING
Warnings & Cautions
Warning or Caution— Consult accompanying documents. Read instructions before
connecting or operating.
Non‑ionizing, electromagnetic radiation
Product Use & Specifications
Refer to the operations & maintenance manual
Refer to the operations & maintenance manual
Manufacturer
Use‑by date
Catalog number
Serial number
Batch code
Temperature limitation
Humidity limitation
Atmospheric pressure limitation
Sterilized through irradiation
Reuse is not allowed
Statement of prescription
41
Operations & Maintenance Manual: Symbol directory
SYMBOL MEANING
Electrical & Power
Class II equipment
Type BF applied part
Energy Efficiency Level V
Direct current
Alternating current
Connector polarity mark—positive
Shipping & Disposal
Do not use if package is damaged
Quantity per box
Standards & Certifications
CE—Marked in accordance with the Medical Device Directive (MDD)
CSA—Canadian Standards Association mark of certification to applicable standards

for electromedical equipment
EC REP—Authorized Representative in the European Community
FCC—Tested to Federal Communications Commission requirements
UL—Underwriters Laboratories Recognized Component certification mark
TUV—Safety approval mark for components or subassemblies
WEEE—Subject to waste electrical and electronic equipment regulations
42
GLOSSARY
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
CSA Canadian Standards Association
EMI Electromagnetic interference
ESD Electrostatic discharge
Essential performance The system performance necessary to achieve freedom from unacceptable risk
F Fahrenheit
FCC Federal Communications Commission (federal agency in U.S.)
ft Foot
GHz Gigahertz
hPa Hectopascal
Hz Hertz
IEC International Electrotechnical Commission
in Inch
IPA Isopropyl alcohol
kHz Kilohertz
kV Kilovolt
m Meter
mAh Milliampere‑hour
MDD Medical Device Directive
MHz Megahertz
mm Millimeter
OSHA Occupational Safety and Health Administration (federal agency in U.S.)
Water that is suitable for high‑level disinfection according to local regulations
Pure water
and your medical facility
RF Radio frequency
UL Underwriters Laboratories
V Volt
Vrms Voltage root mean squared
W Watt
WEEE Waste electrical and electronic equipment
43
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Copyright © 2009, 2016 by Verathon Inc. All rights reserved.

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

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

Precautions & Warnings.......................................................................................................................................2

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

Monitor Controls & Connections .........................................................................................................................9

Video Laryngoscope Components........................................................................................................................9

Procedure 1. Perform Initial Inspection...................................................................................................... 10

Procedure 2. Charge the Monitor.............................................................................................................. 11

Procedure 3. Connect a Video Baton......................................................................................................... 13

Procedure 4. Perform a Functional Check.................................................................................................. 14

USING THE DEVICE.............................................................................................................................................. 15

Procedure 1. Connect a Video Baton......................................................................................................... 16

Procedure 2. Insert the Video Baton into the Stat...................................................................................... 17

Procedure 3. Prepare the System............................................................................................................... 18

Procedure 4. Intubate Using the GlideScope 4‑Step Technique................................................................... 19

Procedure 1. Clean the Video Monitor.......................................................................................................22

Procedure 2. Clean the Video Baton Cradle...............................................................................................22

Procedure 3. Clean the Storage Case.........................................................................................................22

Procedure 1. Remove the Stat...................................................................................................................23

Procedure 2. Clean & Disinfect the Video Baton........................................................................................ 24

Procedure 3. Inspect the Video Baton........................................................................................................26

MAINTENANCE & SAFETY...................................................................................................................................27

GlideScope Ranger Battery.................................................................................................................................27

STATEMENT OF INTENDED USE

NOTICE TO ALL USERS

Verathon recommends that new GlideScope users:

Medical electrical equipment requires special precautions regarding electromagnetic

Cleaning is critical to ensuring a component is ready for disinfection or sterilization. Failure

Do not reuse, reprocess or resterilize single‑use components. Reuse, reprocessing or resterilization

No modification of this equipment is allowed.

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

Do not reuse, reprocess, or resterilize single‑use components. Reuse, reprocessing, or

Figure 1. Ranger Single‑Use System

Video monitor Power supply Power cable

Video baton 1‑2 Video baton 3‑4

Table 2. Optional System Components

Figure 2. Ranger Video Monitor

Video cable connector DC power socket

Battery charge status LED

VIDEO LARYNGOSCOPE COMPONENTS

Video baton Video cable

Camera and light

Procedure 1. PERFORM INITIAL INSPECTION

2. Inspect the components for damage.

Figure 4. Battery Charge Level Icons

Steady green—The battery is fully charged.

No LED—The battery is completely depleted and needs to be recharged.

Flashing orange—There is an issue with the battery.

1. Ensure that the power switch is in the OFF position.

4. Plug the power cord into an AC power outlet.

1. Ensure that the power switch is in the OFF position.

5. Continue to the procedure Perform a Functional Check on page 14.

3. On the video monitor, turn the power switch to the ON position.

Using the system consists of the following procedures:

Table 3. Video Laryngoscope Sizes