ACIST HDi® System Console
ACIST MEDICAL SYSTEMS, INC. · Model 017987
HDi System Console, p/n 701460-007.
Intended use: An assembly of mains electricity (AC-powered) devices designed for extracorporeal and/or intracorporeal (endosonography or endoscopic) imaging procedures involving the heart and blood vessels. Included are software packages that support a variety of static or real-time cardiac specific imaging applications used to diagnose anatomical defects of the heart, determine blood flow characteristics and functional/anatomical problems associated with myocardial infarction. It is used to generate ultrasound pulses, direct them to a target area, detect the echoes, and process the resulting information to produce and display static or dynamic two or three-dimensional (3-D) images.
Key tips
- ·When no category-specific guidance fits, default to the manufacturer's own service manual and the general troubleshooting method in the Engineer's Guide.
- ·Run an incoming and annual electrical safety test regardless of how niche the device is.
Typical Failure Modes
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.
Injector will not arm / fill or delivers inaccurate volume
HighSymptoms: Will not arm, syringe will not fill / advance, flow or volume wrong, stalls under pressure.
Root cause: Air in the syringe / line, a syringe not seated, a drive-motor or plunger fault, or a self-test failure.
Hand-controller / touchscreen fault
MediumSymptoms: No response from the hand controller (AngioTouch) or the console touchscreen, cannot program or start.
Root cause: Hand-controller cable / contacts, or a display fault.
Pressure / occlusion sensing fault
MediumSymptoms: Frequent high-pressure or occlusion alarms with a patent line, or none when the line is blocked.
Root cause: Pressure transducer drift or a manifold / tubing-set issue.
Contrast / saline supply or air-management fault
MediumSymptoms: Air not purged, spike not primed, contrast or saline not drawn.
Root cause: Spike set, air detector, or the priming sequence.
Console cable / communication fault
LowSymptoms: Console and injector head lose communication, will not initialise.
Root cause: Console-to-head cable or a control board.
Serviceable Parts & Consumables
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.
Syringe drive motor / plunger assembly
Class Major service partRel. cost $$$R&R Difficult
Hand controller (AngioTouch)
Class Periodic replacementRel. cost $$R&R Easy
Pressure transducer
Class Periodic replacementRel. cost $$R&R Moderate
Disposable syringe / manifold / tubing set
Class ConsumableRel. cost $R&R Easy
Console cable
Class Periodic replacementRel. cost $$R&R Easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Syringe drive motor / plunger assembly | Major service part | $$$ | Difficult |
| Hand controller (AngioTouch) | Periodic replacement | $$ | Easy |
| Pressure transducer | Periodic replacement | $$ | Moderate |
| Disposable syringe / manifold / tubing set | Consumable | $ | Easy |
| Console cable | Periodic replacement | $$ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
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.
- ·Follow the manufacturer's PM schedule
- ·Perform incoming and annual electrical safety testing per facility biomedical program
Troubleshooting Approach
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.
Symptom: Will not arm / fill
- Purge all air from the syringe and connecting lines.
- Confirm the syringe / manifold set is seated and the plunger is engaged.
- Let the self-tests complete and note any message.
- Substitute a known-good hand controller if that input is suspect.
- If self-tests still fail, refer for service.
Symptom: Pressure / occlusion alarms
- Check the line and manifold for kinks, clamps or a clot.
- Re-prime and re-zero.
- Verify the pressure transducer against a reference if tooling allows.
- Fit a fresh disposable set.
- Replace the transducer if it still misreads.
Technical Specs
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- No
- Single use
- No
- Prescription use
- Rx only
- FDA distribution status
- In Commercial Distribution
- Device type (GMDN)
- Cardiovascular ultrasound imaging system
- FDA product classification
- System, Imaging, Pulsed Echo, Ultrasonic
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Varies by device - check the unit's own manual for facility placement guidance
Documents & Manuals
No documents available for this device yet.
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