LifeHealth · Model IRMA TRUpoint Blood Analysis
• An extensive, flexible test menu enables the portable IRMA TruPoint to be used wherever your patient may be • Operation is easy and room temperature stored cartridges are ready to use anytime, anywhere • Integrated, automatic electronic quality control enhances safety and improves compliance • Complete portability with lightweight, easy grip, and battery operation
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: Aspiration error, short sample, carryover.
Root cause: Clot/crystal obstruction.
Symptoms: Vibration, loud noise, stop error.
Root cause: Worn bearing or unbalanced rotor.
Symptoms: Incubator out of range.
Root cause: Failed heater/fan or sensor.
Symptoms: Low signal, wavelength drift.
Root cause: Lamp/LED or monochromator aging.
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.
Frequent R&R on high-throughput analyzers.
Consumable - replace proactively.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Sample aspiration probe Frequent R&R on high-throughput analyzers. | Periodic replacement | $$$ | Moderate |
| Peristaltic pump tubing Consumable - replace proactively. | Frequent wear item | $ | Easy |
| Xenon / LED light source | Periodic replacement | $$$ | Moderate |
| Centrifuge rotor & bearings | Major service part | $$$ | Difficult |
Relative cost: $ lowest · $$$$ 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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
May report values outside the published performance specifications for pH. After a certain point in shelf life, the pH sensor may give results that are falsely elevated. The discrepancy is greater as shelf life progresses and can be seen on the aqueous controls before the blood.
The barometric pressure measurement output of this particular IRMA TRUPoint SN 443914 device will drift over time.
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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