Do you have a question about the SBM IDRA and is the answer not in the manual?
Details the IDRA device's capabilities for Dry Eye Disease diagnosis and related exams.
Covers warning, reading instructions, careful handling, fragility, and moisture avoidance.
Includes CE marking, manufacturer info, WEEE disposal, and device serial/number references.
Relates to environmental conditions for transport and storage.
Lists crucial warnings for handling, power, liquids, environment, and patient safety.
Provides contact information for software or device issues.
Details maintenance steps, emphasizing power disconnection.
Instructs on storing the instrument and cleaning lenses and surfaces.
Outlines responsibilities for extraordinary maintenance and pre-shipment cleaning.
Specifies environmental conditions for shipment, storage, and use.
Lists examples of replaceable parts for the device.
Details essential or recommended accessories for using the IDRA.
Lists the components included in the instrument's packaging.
Provides step-by-step instructions for installing the IDRA software.
Explains the internet connection and registration process for application activation.
Details how to set and manage a security code for data protection.
Summarizes the main operating characteristics and research behind the IDRA.
Explains how to perform interferometric analysis of the tear film's lipid layer.
Describes examining and measuring the tear meniscus height and shape.
Details how to evaluate tear film stability using NIBUT.
Explains how to capture and analyze meibomian glands images.
Describes the main features and layout of the IDRA software's home screen.
Guides on how to add a new patient's information into the software.
Explains how to initiate a new screening exam for a selected patient.
Details the procedure for capturing and evaluating interferometry videos.
Guides on taking photos and measuring tear meniscus height.
Explains how to record videos for automatic tear film break-up time analysis.
Details the procedure for the Break-Up Time (BUT) exam.
Describes how to capture and analyze meibomian glands images.
Explains how to take pictures for blepharitis assessment with magnification.
Guides on taking pictures using infrared light to observe parasite movement.
Explains how to assess corneal regularity using concentric rings.
Details how to measure pupillary diameter under different light conditions.
Explains how to measure the horizontal iris diameter from white to white.
Describes using the device as a digital slit lamp for anterior segment study.
Explains how to view the list of saved exams for a specific patient.
Differentiates between saved picture and video exam types.
Describes how to add an exam by returning to the main exams screen.
Explains the process for deleting individual or multiple examinations.
Details how to save or print different types of exam reports in PDF format.
Allows adding notes to a selected exam before saving the PDF.
Enables comparison of images/videos with patient data or grading scales.
Starts a timer on the device screen for timing exams.
Automatically sets the correct light quantity for exposure.
Allows manual adjustment of light exposure using ISO settings.
Obtains and maintains automatic focus on the subject.
Allows manual adjustment of the focus on the subject.
Explains how to use and adjust white, blue, and infrared lighting.
Allows manual adjustment of zoom for better patient focus.
Addresses issues with the device not working or LEDs being off.
Provides solutions for the camera display showing a black screen.
Lists the technical specifications of the IDRA device.
Lists the minimum and recommended hardware specifications for the software.
Presents results for radiated emission tests according to EN 55011.
Displays graphs showing radiated emission peaks and limits.
Details the electrostatic discharge immunity test results and standards.
Presents results for radiated electromagnetic immunity tests.
Details immunity test results for RF wireless communication equipment.
Presents results for power frequency magnetic fields immunity test.
Provides a summarized table of all performed tests and their results.
Explains how to set or manage the application pass code.
Describes downloading sample photos and videos for demonstration.
Allows adjustment of video compression, cutoff, and quality.
Provides information about software version and updates.
Verifies the correct working status of the software.
Explains options for single vs. separate databases for users.
Provides technical details about the device hardware.
Details how to input company address and contact for report printing.
Explains how to map a network drive to access the ICP database.
Guides on configuring ICP to use a database located on a network drive.
Provides instructions and regulations for disposing of the electronic equipment.
Details the manufacturer's responsibilities and disclaimers for product use.
Outlines the 12-month warranty coverage and exclusions.
Specifies conditions under which the warranty is void.
Provides contact details for technical maintenance and support.
Declares the device's compliance with EU directives and essential requirements.
Details the IDRA device's capabilities for Dry Eye Disease diagnosis and related exams.
Covers warning, reading instructions, careful handling, fragility, and moisture avoidance.
Includes CE marking, manufacturer info, WEEE disposal, and device serial/number references.
Relates to environmental conditions for transport and storage.
Lists crucial warnings for handling, power, liquids, environment, and patient safety.
Provides contact information for software or device issues.
Details maintenance steps, emphasizing power disconnection.
Instructs on storing the instrument and cleaning lenses and surfaces.
Outlines responsibilities for extraordinary maintenance and pre-shipment cleaning.
Specifies environmental conditions for shipment, storage, and use.
Lists examples of replaceable parts for the device.
Details essential or recommended accessories for using the IDRA.
Lists the components included in the instrument's packaging.
Provides step-by-step instructions for installing the IDRA software.
Explains the internet connection and registration process for application activation.
Details how to set and manage a security code for data protection.
Summarizes the main operating characteristics and research behind the IDRA.
Explains how to perform interferometric analysis of the tear film's lipid layer.
Describes examining and measuring the tear meniscus height and shape.
Details how to evaluate tear film stability using NIBUT.
Explains how to capture and analyze meibomian glands images.
Describes the main features and layout of the IDRA software's home screen.
Guides on how to add a new patient's information into the software.
Explains how to initiate a new screening exam for a selected patient.
Details the procedure for capturing and evaluating interferometry videos.
Guides on taking photos and measuring tear meniscus height.
Explains how to record videos for automatic tear film break-up time analysis.
Details the procedure for the Break-Up Time (BUT) exam.
Describes how to capture and analyze meibomian glands images.
Explains how to take pictures for blepharitis assessment with magnification.
Guides on taking pictures using infrared light to observe parasite movement.
Explains how to assess corneal regularity using concentric rings.
Details how to measure pupillary diameter under different light conditions.
Explains how to measure the horizontal iris diameter from white to white.
Describes using the device as a digital slit lamp for anterior segment study.
Explains how to view the list of saved exams for a specific patient.
Differentiates between saved picture and video exam types.
Describes how to add an exam by returning to the main exams screen.
Explains the process for deleting individual or multiple examinations.
Details how to save or print different types of exam reports in PDF format.
Allows adding notes to a selected exam before saving the PDF.
Enables comparison of images/videos with patient data or grading scales.
Starts a timer on the device screen for timing exams.
Automatically sets the correct light quantity for exposure.
Allows manual adjustment of light exposure using ISO settings.
Obtains and maintains automatic focus on the subject.
Allows manual adjustment of the focus on the subject.
Explains how to use and adjust white, blue, and infrared lighting.
Allows manual adjustment of zoom for better patient focus.
Addresses issues with the device not working or LEDs being off.
Provides solutions for the camera display showing a black screen.
Lists the technical specifications of the IDRA device.
Lists the minimum and recommended hardware specifications for the software.
Presents results for radiated emission tests according to EN 55011.
Displays graphs showing radiated emission peaks and limits.
Details the electrostatic discharge immunity test results and standards.
Presents results for radiated electromagnetic immunity tests.
Details immunity test results for RF wireless communication equipment.
Presents results for power frequency magnetic fields immunity test.
Provides a summarized table of all performed tests and their results.
Explains how to set or manage the application pass code.
Describes downloading sample photos and videos for demonstration.
Allows adjustment of video compression, cutoff, and quality.
Provides information about software version and updates.
Verifies the correct working status of the software.
Explains options for single vs. separate databases for users.
Provides technical details about the device hardware.
Details how to input company address and contact for report printing.
Explains how to map a network drive to access the ICP database.
Guides on configuring ICP to use a database located on a network drive.
Provides instructions and regulations for disposing of the electronic equipment.
Details the manufacturer's responsibilities and disclaimers for product use.
Outlines the 12-month warranty coverage and exclusions.
Specifies conditions under which the warranty is void.
Provides contact details for technical maintenance and support.
Declares the device's compliance with EU directives and essential requirements.
| Brand | SBM |
|---|---|
| Model | IDRA |
| Category | Medical Equipment |
| Language | English |