GN Otometrics · Model CHARTR 200 VNG
• Portable full diagnostic system for USB connection with laptop • Lightweight, comfortable goggles with fixation light • Proven VNG eye-tracking algorithm eliminates errors due to eye blinks. • Built-in Video Recorder and Video Playback • Quick review of eye movement tracings • Integrated analysis and normative data displays • Built-in report template with Interpretation Assistant • Complete test battery including saccades, pursuit, optokinetics, gaze, positional, Hallpike, and calorics. • Extensive library of test protocols for custom test batteries
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.
Consumable.
High-value, track usage.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Peristaltic pump tubing Consumable. | Frequent wear item | $ | Easy |
| Imaging camera module | Periodic replacement | $$$ | Difficult |
| Phaco handpiece / tip High-value, track usage. | Periodic replacement | $$$$ | Difficult |
| Illumination lamp / LED | Periodic replacement | $$$ | 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 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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
There is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock.
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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