
Haag-Streit · Model Octopus 300
The Octopus 300 is the compact perimeter for every glaucoma practice. It even fits in a corner and produces accurate results without a dark room. The Octopus 300 incorporates both Short-Wavelength Automated Perimetry (SWAP) and Flicker Perimetry for early glaucoma detection. Central field standard white-on-white perimetry Automatically recognizes fixation losses Fast-thresholding strategy Cluster analysis - high sensitivity and specificity EyeSuite Perimetry software - included Octopus Blink Control Pupil position control Automated eye tracking Contact control Printout and graphics representation results.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Stimuli not projected, wrong intensity, uneven bowl illumination, fixation target not visible.
Root cause: Projection / bowl-illumination LED or lamp at end of life, a filter / shutter fault, or the projection mechanism.
Symptoms: Excessive fixation losses, the eye / video monitor blank, gaze check will not calibrate.
Root cause: Eye-monitor camera / IR illuminator, or head / chin positioning.
Symptoms: Response-button presses not registered.
Root cause: Response button or cable fault.
Symptoms: Chin rest / trial-lens holder will not move to command.
Root cause: Positioning drive motor or its control.
Symptoms: Tests will not save, transfer (EyeSuite) or print.
Root cause: PC, network, or printer.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Projection / bowl-illumination LED / lamp | Periodic replacement | $$ | Moderate |
| Filter / shutter assembly | Major service part | $$$ | Difficult |
| Eye-monitor camera / IR illuminator | Major service part | $$ | Moderate |
| Response button / cable | Periodic replacement | $ | Fairly easy |
| Chin-rest / trial-lens-holder drive | Major service part | $$ | Moderate |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Synced live from the FDA openFDA API.
Software error -Software REF 615 588 versions 2.0 to 3.3, movement of the focusing is triggered by pressing the button of the footswitch it might occur that the movement does not stop when releasing the button, result in potential risk to the patient's eye
The firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.
Currently there is a possibility, at the start of the perimetry examination, for the background illumination of the cupola not to turn on. If no illumination of cupola occurs, data obtained from the examination could provide the doctor with results that would appear to be better than actual.
A patient record may be linked to an incorrect/inconsistent set of calculation results under specific circumstances when using EyeSuite Software version i2.000.
During the creation of the Lenstar LS 900 software, the ability to perform a manual adjustment of the retinal thickness measurement was not disabled for products targeted for US distribution. The current software installed allows the user to manually alter the retinal thickness measurement, which could modify the automatic axial eye length measurement resulting in the selection of an incorrect in
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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