What to do if temperature monitoring error occurs in Zeiss VISULAS green?
If the temperature within the Zeiss Medical Equipment laser console is too high, ensure that the vent slots on the laser console are not covered and that the ambient temperature is below 35 °C.
What to do if Zeiss VISULAS green says 'Fiber not connected'?
If the Zeiss Medical Equipment shows that the fiber is not connected, check that the optical fiber is properly inserted and screwed in tightly.
What to do if I get a connection error of physician's safety filter on my Zeiss VISULAS green?
If there is a connection error of the physician's safety filter on your Zeiss Medical Equipment, check that the slit lamp and the OPMI (ENDO physician's safety filter) are correctly connected and properly inserted.
What to do if Zeiss Medical Equipment says 'Trigger not connected'?
If the Zeiss Medical Equipment indicates that the trigger is not connected, verify that the foot switch and the slit lamp are correctly connected and properly inserted.
How to fix door switch issue on Zeiss VISULAS green Medical Equipment?
If there is a problem with the door switch on the Zeiss Medical Equipment, ensure the door is shut or check that the shorting plug is correctly plugged into the yellow socket.
What to do if the laser stop switch is locked on Zeiss VISULAS green?
If the laser stop switch is locked on the Zeiss Medical Equipment, unlock the laser stop switch.
Why does 'DEMO treatment' appear instead of 'Treat' on my Zeiss VISULAS green?
If the 'DEMO treatment' work step appears instead of the 'Treat' work step and the laser cannot be triggered on your Zeiss Medical Equipment, deactivate the DEMO mode by pressing the [DEMO] button under "Settings / System / Information".
What to do if Zeiss VISULAS green says 'Trigger pressed'?
If the trigger is pressed on the Zeiss Medical Equipment, release the trigger to continue, as it is not permitted to switch to treatment mode while the trigger is pressed for safety reasons.
What to do if ERROR log deactivated on Zeiss VISULAS green?
Please contact ZEISS Service if the ERROR log is deactivated on your Zeiss Medical Equipment, and remember that patients must not be treated in this mode!
What to do if the Zeiss Medical Equipment shows a power warning?
If the internal monitoring of your Zeiss Medical Equipment identifies that the actual laser power output deviates from the target power output selected on the control panel by more than 20 %, this triggers a power warning. If this warning repeats, notify ZEISS Service.
Defines the applicability of the VISULAS green system.
Explains the purpose of the manual and its storage guidelines.
Provides contact information for inquiries and feedback.
Details conventions for lists, cross-references, and highlighted text.
Explains conventions for warnings, cautions, notes, prerequisites, and actions.
Lists other relevant documents for additional components and accessories.
Specifies the qualifications and training required for system operators.
Details the system's intended use and limitations for eye treatments.
Specifies the medical conditions for which the device is indicated.
Lists potential side effects and conditions where the device is contraindicated.
Defines the obligations of the organization operating the system.
Outlines essential safety measures and responsibilities for system operators.
Covers risks associated with both incoherent and coherent laser radiation.
Addresses precautions to prevent fire hazards during system operation.
Provides guidelines to prevent damage to fiber optic components.
Specifies requirements for system maintenance and repairs.
Lists the components included in different VISULAS green system versions.
Explains the various labels and symbols found on the laser console and components.
Illustrates the overall system configuration and interconnections.
Identifies and explains the function of system controls and ports.
Explains the basic principles of laser beam generation.
Highlights critical safety precautions during system installation.
Provides instructions and warnings for connecting system parts.
Details the procedure for attaching the foot switch to the instrument table.
Explains safe procedures for relocating the instrument table.
Outlines daily pre-use checks to ensure system readiness and safety.
Describes the procedure for powering on the VISULAS green system.
Lists critical safety warnings and precautions during system operation.
Guides the user through the process of using the laser with a slit lamp.
Guides the user on connecting and operating the system with laser endoprobes.
Outlines the correct procedure for powering down the VISULAS green system.
Discusses measures for protecting system data and user information.
Introduces the main elements of the control panel's user interface.
Explains how to use the on-screen keyboard for data entry.
Details how to set up basic treatment parameters before starting.
Guides the user in setting specific laser parameters for treatment.
Describes how to activate the laser and adjust parameters during active treatment.
Explains how to view, export, and save treatment data and reports.
Covers configuration options for language, treatments, contact lenses, system info, and maintenance.
Highlights hazards related to moisture and cross-contamination during cleaning.
Provides instructions on how to clean device components safely.
Explains the procedure for disinfecting patient-contact parts.
Details procedures for checking protective earth resistance and insulation.
Outlines the requirements for annual safety inspections of the device.
Step-by-step guide for replacing the slit lamp's halogen bulb.
Instructions for safely replacing fuses in the laser console.
Guide for replacing the optional fixation lamp's LED.
Lists error messages and their corresponding causes and remedies.
Covers system messages that do not trigger audible alerts or error codes.
Directs users to find local ZEISS representatives online.
Lists key performance features critical for safe and effective operation.
States the UMDNS number and laser class of the system.
Provides detailed technical data for the laser system.
Lists technical specifications for the LSL green laser slit lamp.
Specifies operating and storage environmental requirements.
Details EMC guidelines, emissions, and immunity standards.
Covers safety and connection aspects related to instrument tables.
Details specifications and usage recommendations for laser endoprobes.
Explains how to connect the door contact isolator for safety interlocks.
Describes the importance and types of physician's safety filters.
Provides guidelines for environmentally responsible disposal of the system and its components.
General| Wavelength | 532 nm |
|---|---|
| Cooling | Air-cooled |
| Laser Type | Frequency-doubled Nd:YAG |
| Power at the cornea | Up to 1.5 W |
| Spot Size | 50 - 500 µm |
| Treatment Modes | Single, Continuous Wave (CW) |
| Aiming Beam | 635 nm, adjustable brightness |
| Electrical Requirements | 100 - 240 V, 50/60 Hz |
| Application | Retinal photocoagulation |
| Slit Lamp Compatibility | ZEISS slit lamps, Haag-Streit slit lamps (with adapter) |
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