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Covers critical safety warnings regarding installation, operation, and handling.
Provides an overview of the manual's structure and content sections.
Details safety measures for installing, operating, and handling the instrument.
Instructions for verifying all items are present and undamaged upon receiving the package.
Defines technical terms and abbreviations used throughout the manual.
Provides a step-by-step overview of the instrument's primary measurement process.
Identifies and explains controls and parts visible from the operator's perspective.
Identifies and explains parts related to patient interaction and instrument connection.
Details all indicators, icons, and display fields on the instrument's screen.
Explains the operation of the joystick for positioning the measuring head.
Explains the touch panel feature for aligning the instrument with the patient's eye.
Details the RS-232C port for external device connectivity and associated precautions.
Explains the meaning of various symbols found on the instrument and in the manual.
Essential safety guidelines for instrument installation and power connection.
Steps to take before initiating an intraocular pressure measurement.
The core process of taking intraocular pressure readings.
Details on how to print measurement results.
Procedures for recalling and reviewing measurement data stored in the instrument's memory.
Steps to input patient identification for data communication purposes.
Configuring permanent settings for operation, time, units, and output.
Explains how central corneal thickness affects IOP readings and adjustment methods.
Presents data and results from device performance tests under controlled models.
Summarizes clinical trial results and comparison with Goldmann applanation tonometer.
Details the terms and conditions of the product's limited warranty.
Information on the instrument's expected lifespan and initial inspection procedures.
Procedures for performing routine inspections of the instrument.
Guidelines for cleaning the critical measurement window to ensure accuracy.
Instructions for replacing the printer paper roll when needed.
Proper procedures for storing the instrument when not in use to maintain its condition.
Instructions for the safe and environmentally responsible disposal of the instrument.
Technical details on the range and increments for IOP measurement.
Details on the printer, movement strokes, display, dimensions, and weight.
Information on light sources, wavelengths, and power output for instrument operation.
Specifications for instrument noise levels.
Recommended environmental conditions for operating and storing the instrument.
Details product classification, protection against electric shock, and operational mode.
Statement regarding electromagnetic compatibility and compliance with relevant standards.
Covers critical safety warnings regarding installation, operation, and handling.
Provides an overview of the manual's structure and content sections.
Details safety measures for installing, operating, and handling the instrument.
Instructions for verifying all items are present and undamaged upon receiving the package.
Defines technical terms and abbreviations used throughout the manual.
Provides a step-by-step overview of the instrument's primary measurement process.
Identifies and explains controls and parts visible from the operator's perspective.
Identifies and explains parts related to patient interaction and instrument connection.
Details all indicators, icons, and display fields on the instrument's screen.
Explains the operation of the joystick for positioning the measuring head.
Explains the touch panel feature for aligning the instrument with the patient's eye.
Details the RS-232C port for external device connectivity and associated precautions.
Explains the meaning of various symbols found on the instrument and in the manual.
Essential safety guidelines for instrument installation and power connection.
Steps to take before initiating an intraocular pressure measurement.
The core process of taking intraocular pressure readings.
Details on how to print measurement results.
Procedures for recalling and reviewing measurement data stored in the instrument's memory.
Steps to input patient identification for data communication purposes.
Configuring permanent settings for operation, time, units, and output.
Explains how central corneal thickness affects IOP readings and adjustment methods.
Presents data and results from device performance tests under controlled models.
Summarizes clinical trial results and comparison with Goldmann applanation tonometer.
Details the terms and conditions of the product's limited warranty.
Information on the instrument's expected lifespan and initial inspection procedures.
Procedures for performing routine inspections of the instrument.
Guidelines for cleaning the critical measurement window to ensure accuracy.
Instructions for replacing the printer paper roll when needed.
Proper procedures for storing the instrument when not in use to maintain its condition.
Instructions for the safe and environmentally responsible disposal of the instrument.
Technical details on the range and increments for IOP measurement.
Details on the printer, movement strokes, display, dimensions, and weight.
Information on light sources, wavelengths, and power output for instrument operation.
Specifications for instrument noise levels.
Recommended environmental conditions for operating and storing the instrument.
Details product classification, protection against electric shock, and operational mode.
Statement regarding electromagnetic compatibility and compliance with relevant standards.
General| Corneal topography | Yes |
|---|---|
| Pachymetry | Yes |
| Anterior chamber depth | Yes |
| Keratometry | Yes |
| Pupillometry | Yes |
| Power Supply | AC 100-240V, 50/60 Hz |
| Measurement Principle | Optical Coherence Tomography (OCT) |
| Scan Time | 1.5 seconds |
| Display | 10.4-inch color LCD |
| Power Consumption | 100VA |
