Heidelberg Engineering · Model Spectralis HRA
Diagnostic Imaging Platform The SPECTRALIS® HRA ophthalmic imaging platform is especially designed for dye-based angiography such as Fluorescein Angiography (FA) and is equipped with several scanning laser fundus imaging modalities. As an expandable platform, it can be upgraded any time with additional scanning laser fundus imaging modalities, such as ICGA imaging, the Ultra-Widefield Angiography Module or the MultiColor Module. The SPECTRALIS HRA is always delivered with a panning camera head and an external touch panel control for easy adjustment and acquisition that in particular facilitates dye-based angiography with FA or ICGA.
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Symptoms: Dim illumination, lamp error.
Root cause: Xenon/LED aging.
Symptoms: No phaco power, error.
Root cause: Tip or handpiece wear.
Symptoms: Unstable anterior chamber.
Root cause: Peristaltic pump wear.
Symptoms: Blurry/offset image.
Root cause: Camera calibration drift.
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
High-value, track usage.
Consumable.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Phaco handpiece / tip High-value, track usage. | Periodic replacement | $$$$ | Difficult |
| Illumination lamp / LED | Periodic replacement | $$$ | Moderate |
| Peristaltic pump tubing Consumable. | Frequent wear item | $ | Easy |
| Imaging camera module | Periodic replacement | $$$ | Difficult |
Relative cost: $ lowest · $$$$ 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 structured starting point derived from the failure modes above. 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.
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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