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Display Type | LCD |
---|---|
Power Source | Rechargeable lithium-ion battery |
Storage Temperature | -20°C to 60°C (-4°F to 140°F) |
Altitude | Up to 3000 m (9842 ft) |
Relative Humidity | 15% to 95% non-condensing |
Contact details for Verathon Inc. in Bothell, WA, USA.
Contact details for Verathon Medical (Canada) ULC in Burnaby, BC, Canada.
Contact details for Verathon Medical (Europe) B.V. in Amsterdam, Netherlands.
Contact details for Verathon Medical (Australia) Pty Limited in St Leonards, NSW, Australia.
Contact details for MDSS CH GmbH in Aarau, Switzerland (CH REP).
Contact details for Anandic Medical Systems AG in Feuerthalen, Switzerland.
Describes the GlideScope Go 2 system features, including blades and Stats.
Overview of the GlideScope Go 2 handheld video laryngoscope system's capabilities.
Specifies the intended use of the GlideScope Go 2 System by qualified medical professionals.
Legal restriction on device sale in the US, requiring physician order.
Important recommendations for all users, including training and practice.
Warnings related to checking instrument condition, modifications, and safe handling during use.
Warnings concerning product contamination and compliance with safety standards during reprocessing.
Warnings about electric shock hazards and using only Verathon-specified accessories.
Warning regarding system incompatibility with magnetic resonance imaging (MRI) environments.
Cautions regarding initial cleaning, electromagnetic compatibility, and proper USB port usage.
Lists incompatible part numbers and handling precautions for single-use items.
EU specific reporting requirement for serious incidents to authorities.
Illustrates and lists the essential parts required for the GlideScope Go 2 system.
Illustrates and lists optional parts and accessories for the GlideScope Go 2 system.
Explains the function of buttons and icons on the monitor interface for operation.
Identifies physical components and ports on the Go 2 monitor.
Describes the layout and features displayed on the Home screen for system information access.
Steps for initial system setup including inspection, charging, wizard, settings, and attachment.
Instructions for charging the monitor battery before initial use, including status indicators.
Guide to initial system configuration for language, date, and time.
Steps to customize system settings like snapshot, video, and automatic shutdown preferences.
How to manage device storage, export, and remove media files.
Options to configure system language, date, and time settings.
Settings for device name, security code, and importing/exporting configurations.
Information on hardware, software upgrades, and usage statistics.
How to prepare the video baton for use with a GVL Stat.
Instructions for connecting the video baton or blade to the monitor.
Steps to verify the system is working correctly before use.
Steps to prepare the system before use, including cleaning and attachment.
Detailed guide on the GlideScope 4-Step Technique for intubation.
How to enable/disable and use Dynamic Light Control for image optimization.
Instructions for manual and automatic video recording and snapshot capture.
Steps to safely disconnect the scope from the monitor.
How to safely remove and dispose of a single-use Stat from a video baton.
Guide to exporting and optionally encrypting video and snapshot files to a USB drive.
Reference to guidelines for cleaning, disinfection, and sterilization of components.
Information on no required inspections and details on battery life and replacement.
Guidance on software updates, device repair, and proper disposal of the system.
Details the limited warranty for the GlideScope Go 2 monitor, including scope and exclusions.
Steps for requesting service and contacting the customer care department.
Describes Verathon's service quality and options for purchasing extended warranties.
Legal explanation of customer rights and limitations of warranties.
Detailed technical specifications for the GlideScope Go 2 monitor, including dimensions and performance.
Guidance and declaration regarding the system's immunity to electromagnetic disturbances.
Further details on electromagnetic immunity testing and recommended environments.
Declaration of the system's RF emissions and suitability for healthcare environments.
Information on using specified accessories to maintain EMC compliance.
Definitions of specialized terms used in the manual and on the product.