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GLIDESCOPE TITANIUM REUSABLE & SPECTRUM SINGLE‑USE Operations & Maintenance Manual Effective: April 23, 2020 Caution: Federal (United States) law restricts this device to sale by or on the order of a physician. 0900‑4712 REV‑08...
TABLE OF CONTENTS IMPORTANT INFORMATION ..........................1 Product Information ............................1 Product Description ............................1 Statement of Intended Use ..........................1 Essential Performance ............................1 Environments of Intended Use..........................1 Statement of Prescription ............................1 Notice to All Users ..............................2 Warnings & Cautions ............................2 INTRODUCTION ..............................7 Titanium Reusable & Spectrum Single‑Use Systems .....................7 System Parts &...
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USING THE DEVICE .............................26 Procedure 1. Prepare the GlideScope System .................... 27 Procedure 2. Intubate the Patient ......................28 Procedure 3. Use the Record & Snapshot Features (Optional) ..............29 Procedure 4. Use the Playback Feature (Optional) ..................31 Procedure 5. Prepare a Component for Cleaning ..................32 REPROCESSING ..............................33 MAINTENANCE &...
ESSENTIAL PERFORMANCE Essential performance is the system performance necessary to achieve freedom from unacceptable risk. The essential performance of the GlideScope Titanium Reusable and Spectrum Single‑Use systems is to provide a clear view of the vocal cords. ENVIRONMENTS OF INTENDED USE The GlideScope Titanium Reusable and Spectrum Single‑Use systems are intended to be used in professional...
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.
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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/global‑support. WARNING For information on the handling and disposing of recommended reprocessing solutions, please refer to the solution manufacturer’s instructions.
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Verathon. WARNING Electric shock hazard. Do not attempt to open the system components. This may cause serious injury to the operator or damage to the instrument and voids the warranty. Contact Verathon Customer Care for all servicing needs. WARNING Electric shock hazard. Do not immerse the power adapter in water. When cleaning the power adapter, use a cloth dampened with isopropyl alcohol on the outside of the enclosure.
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Use only the accessories and peripherals recommended by Verathon. WARNING Use of accessories and cables other than those specified or provided by Verathon may cause this system to experience electromagnetic malfunctions, including increased emissions or decreased immunity. This may cause improper operation, procedure delays, or both.
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The system contains electronics that may be damaged by ultrasonic and automated washing equipment. Do not use an ultrasonic device or automated washing equipment, other than Verathon‑approved systems, to clean this product. CAUTION When cleaning video laryngoscopes, do not use metal brushes, abrasive brushes, scrub pads, or rigid tools.
Single‑use video laryngoscopes in S3 and S4 sizes may also be available in white. These are not part of the Spectrum Single‑Use system. For more information about the white video laryngoscopes, see the GlideScope Titanium Single‑Use Operations and Maintenance Manual at verathon.com/product‑documentation. TITANIUM REUSABLE SYSTEM The reusable system features a titanium video laryngoscope that must be cleaned and high‑level disinfected...
SYSTEM PARTS & ACCESSORIES Table 1. Required System Components REQUIRED PARTS & ACCESSORIES GlideScope Video Monitor Video cable Spectrum Smart Cable (for reusable system) (for single‑use system) Note: Cable shortened for Note: Cable shortened for illustration purposes. illustration purposes. One or more of the following video laryngoscopes: Spectrum Single‑Use Sizes LoPro S1 LoPro S2...
The 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, see verathon.com/global‑support.
VIDEO LARYNGOSCOPE COMPONENTS The main components of the system are the LoPro, Miller, or Mac video laryngoscopes in either single‑use or reusable configurations. The single‑use video laryngoscopes are available in a disposable format with blades that feature the signature GlideScope LoPro curve, or in Miller and Mac styles which incorporate the look and feel of traditional Miller and Macintosh blades.
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 0900‑4712 REV‑08...
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Table 5. 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...
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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.
1. Verify that you have received the appropriate components for your system by referring to the packing list included with the system. 2. Inspect the components for damage. 3. If any of the components are missing or damaged, notify the carrier and Verathon Customer Care or your local representative. For contact information, visit verathon.com/global‑support. 0900‑4712 REV‑08...
PRoCEdURE 2. MoUNT THE SYSTEM (oPTIoNAL) If you choose to mount the system, you may use either of the following configurations: • Mount it on a premium cart or mobile stand (Figure 6 Figure 7). These solutions make it easy for you to move the system from one location to another.
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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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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 AdJUST THE MoNIToR ANGLE Before you start using the video monitor, adjust the angle of the monitor for optimal viewing.
Warnings & Cautions section before performing the following task. The GlideScope Video Monitor includes an internal lithium‑ion battery. Verathon recommends that you charge the battery fully prior to first use. Under normal operating conditions, a fully charged battery lasts approximately 90 minutes or longer before it needs to be recharged.
The monitor is also compatible with GlideScope AVL system components. For more information, contact Verathon Customer Care or see the GlideScope AVL Single‑Use Operations and Maintenance Manual. OptiOn 1.
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OptiOn 2. SpECtRUM SinGLE‑USE SYStEM IMPORTANT Spectrum Miller video laryngoscopes are not compatible with the original GlideScope Titanium Smart Cable (part number 0800‑0522). You must use a Spectrum Smart Cable (part number 0800‑0543) to connect these video laryngoscopes to a GlideScope Video Monitor. Spectrum Smart Cables can be identified by the blue color of their video laryngoscope connectors.
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5. To disconnect the Smart Cable from the monitor, rotate the connector ring in the direction of the release arrow, and then remove the connector from the port. Connector ring 6. To disconnect a video laryngoscope from the Smart Cable, hold the cable connector in one hand and the video laryngoscope handle in the other, and then pull.
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 to the resolution of the external monitor.
PRoCEdURE 6. CoNFIGURE USER SETTINGS You may configure the following settings directly on the unit: • Date and Time • Audio Recording • Date and Time Format • Auto Recording • Key Click Sound • Auto External Video • Auto Power Off •...
Before you use the device for the first time, perform the following functional check to ensure that the system is working properly. Please contact your local Verathon representative or Verathon Customer Care if your system does not function as described below. For contact information, visit verathon.com/global‑support.
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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.
USING THE DEVICE Prior to using the device, set up the device according to the instructions in the previous chapter, and verify the setup by completing the procedure Perform a Functional Check. Please read the Warnings & Cautions section before performing the following tasks. Titanium video laryngoscopes are equipped with the Reveal anti‑fog feature, which reduces camera fogging during the intubation procedure.
Ensure that each component has been properly cleaned, disinfected, or sterilized according to the guidance provided in the GlideScope and GlideRite Products Reprocessing Manual (part number 0900‑5032), which is available at verathon.com/product‑documentation. In this procedure, you select and attach the appropriate video laryngoscope for the patient, turn the system on, and verify that the system is functioning properly.
Warnings & Cautions section before performing the following tasks. To perform an intubation, Verathon recommends using one of the following techniques appropriate for the style laryngoscope being used. Prior to beginning this procedure, verify that the monitor is receiving an accurate image from the video laryngoscope.
PRoCEdURE 3. USE THE RECoRd & SNAPSHoT FEATURES (oPTIoNAL) Please read the Warnings & Cautions section before performing the following task. The system is equipped with video and audio recording features and the ability to save a snapshot of the live display on the monitor.
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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.
PRoCEdURE 4. 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 35.
PRoCEdURE 5. PREPARE A CoMPoNENT FoR CLEANING 1. Make sure the video monitor has been turned off. 2. Detach the cable from the monitor by turning the connector ring in the direction of the release arrow. Connector ring 3. Detach the cable from the video laryngoscope. If you are cleaning a reusable system, rotate the connector ring on the video cable in the direction of the release arrow and pull the components apart gently.
For information about the cleaning, disinfection, and sterilization requirements for these components, refer to the GlideScope and GlideRite Products Reprocessing Manual (part number 0900‑5032), which is available at verathon.com/product‑documentation. Operations & Maintenance Manual: Reprocessing 0900‑4712 REV‑08...
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.
Product to Verathon (cleaned and disinfected as appropriate) immediately upon receiving the loaner unit from Verathon. Buyer shall return the loaner unit within two (2) business days of receipt of the repaired Product. All exchanged parts become property of Verathon.
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European Customers, any terms herein limiting Verathon’s liability shall not apply insofar as they conflict with mandatory statutory provisions of the Product Liability Act.
PRODUCT SPECIFICATIONS COMPONENT SPECIFICATIONS Table 6. GlideScope Video Monitor (0570‑0338) GENERAL SPECIFICATIONS Classification: Electrical Class II, Applied Part BF Range: 100–240 VAC, 50 and 60 Hz. Connect to a medical‑grade power supply (If Line voltage: the provided power cord has a third prong, it is used as a functional ground). DC power supply: 12 V DC, 3.33 A max Ingress protection:...
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Table 18. Spectrum Miller S1 (Sterile, 0574‑0203; Non‑Sterile, 0574‑0217; Single‑Use System) GENERAL SPECIFICATIONS Ingress protection: IPX4 Expected product life: Refer to the “use by” date indicated by the symbol on the package label. OPERATING & STORAGE SPECIFICATIONS Operating Conditions Shipping & Storage Conditions Temperature: 10–40°C (50–104°F) ‑20–45°C (‑4–113°F)
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Table 20. Spectrum LoPro S2 (Sterile, 0574‑0166; Non‑Sterile, 0574‑0219; Single‑Use System) GENERAL SPECIFICATIONS Ingress protection: IPX4 Expected product life: Refer to the “use by” date indicated by the symbol on the package label. OPERATING & STORAGE SPECIFICATIONS Operating Conditions Shipping & Storage Conditions Temperature: 10–40°C (50–104°F) ‑20–45°C (‑4–113°F)
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Table 22. Spectrum LoPro S3 (Sterile, 0574‑0194; Non‑Sterile, 0574‑0221; Single‑Use System) GENERAL SPECIFICATIONS Ingress protection: IPX4 Expected product life: Refer to the “use by” date indicated by the symbol on the package label. OPERATING & STORAGE SPECIFICATIONS Operating Conditions Shipping & Storage Conditions Temperature: 10–40°C (50–104°F) ‑20–45°C (‑4–113°F)
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Table 24. Spectrum DirectView MAC S3 (Sterile, 0574‑0187; Non‑Sterile, 0574‑0223; Single‑Use System) GENERAL SPECIFICATIONS Ingress protection: IPX4 Expected product life: Refer to the “use by” date indicated by the symbol on the package label. OPERATING & STORAGE SPECIFICATIONS Operating Conditions Shipping &...
BATTERY SPECIFICATIONS Table 26. Battery Specifications CONDITION DESCRIPTION Battery type Lithium‑ion Under normal operating conditions, a fully charged battery lasts Battery life approximately 90 minutes Charging time off line will take no more than 6 hours from an empty battery Charging time to a full charge Rated capacity 2150 mAh...
ELECTROMAGNETIC COMPATIBILITY The system is designed to be in compliance with IEC 60601‑1‑2, which contains electromagnetic compatibility (EMC) requirements for medical electrical equipment. The limits for emissions and immunity specified in this standard are designed to provide reasonable protection against harmful interference in a typical medical installation.
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ELECTROMAGNETIC IMMUNITY Table 28. 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. COMPLIANCE ELECTROMAGNETIC ENVIRONMENT IMMUNITY TESTS...
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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 Component Specifications sections.
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.
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TERM DEFINITION OSHA Occupational Safety and Health Administration (federal agency in U.S.) psia Pounds per square inch absolute Water that is suitable for high‑level disinfection according to local regulations Pure water and your medical facility Radio frequency Relative humidity Restriction of the Use of Certain Hazardous Substances in Electrical and RoHS Electronic Equipment Sodium dodecyl sulphate...
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