OmniVersa
ACCELERATED CARE PLUS CORP · Model 100FXF
Combination electrical stimulation/ultrasound for physical therapy
Intended use: An electrically-powered device assembly intended to apply various modes of electrical stimulation transcutaneously to treat/prevent neuromuscular symptoms and disorders typically as a form of physical therapy [neuromuscular electrical stimulation (NMES)/electronic muscle stimulation (EMS)]; it may in addition be intended for transcutaneous electrical nerve stimulation (TENS) to treat pain, and/or electroacupuncture. It includes an electric current pulse generator and noninvasive electrodes; it is not intended for tremor suppression. Clinical applications typically include relaxation/re-education of muscles, prevention of muscle atrophy, and improvement of blood circulation.
Key tips
- ·Never bypass a radiation interlock to "just get the image" - this is one of the few true zero-tolerance rules in BMET work.
- ·Trend image-quality phantom results over time - drift shows up before an outright failure does.
- ·Portable/mobile units take real physical abuse from transport - check wheel locks and cable strain reliefs more often than fixed units.
Typical Failure Modes
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.
Transducer element failure
MediumSymptoms: Dropout, dead elements, image banding.
Root cause: Element delamination or cable damage from repeated use.
Transducer cable / connector wear
MediumSymptoms: Intermittent image loss, connector-wiggle artifact.
Root cause: Repeated flexing and connector strain.
Recon / system software hang
LowSymptoms: Frozen console, acquisition timeout.
Root cause: Workstation or storage degradation.
Display panel degradation
LowSymptoms: Dim image, color shift, dead pixels.
Root cause: Backlight or LCD panel aging.
Serviceable Parts & Consumables
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.
Ultrasound transducer / probe
Handle with care; most-replaced probe assembly.
Class Periodic replacementRel. cost $$$$R&R Moderate
Transducer cable assembly
Class Periodic replacementRel. cost $$R&R Fairly easy
Workstation / GPU
Class Periodic replacementRel. cost $$$R&R Difficult
Display panel
Class Major service partRel. cost $$R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Ultrasound transducer / probe Handle with care; most-replaced probe assembly. | Periodic replacement | $$$$ | Moderate |
| Transducer cable assembly | Periodic replacement | $$ | Fairly easy |
| Workstation / GPU | Periodic replacement | $$$ | Difficult |
| Display panel | Major service part | $$ | Moderate |
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.
- ·Daily QC per modality: image-quality phantom test
- ·Tube and detector inspection
- ·Annual state-required radiation safety survey
- ·Vendor-scheduled preventive maintenance
Troubleshooting Approach
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Transducer element failure
- Confirm the presentation - typically dropout, dead elements, image banding - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: element delamination or cable damage from repeated use.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the ultrasound transducer / probe per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: Transducer cable / connector wear
- Confirm the presentation - typically intermittent image loss, connector-wiggle artifact - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: repeated flexing and connector strain.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the transducer cable assembly per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Technical Specs
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- No
- Single use
- No
- FDA distribution status
- In Commercial Distribution
- Device type (GMDN)
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- FDA product classification
- Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat; Stimulator, Nerve, Transcutaneous, For Pain Relief; Stimulator, Muscle, Powered
- Manufacturer support
- 800-850-1100 · acp-customersupport@hanger.com
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Radiology / Imaging department
- Emergency Department (portable units)
- Operating Room (C-arms)
- Cath lab
- Bedside ICU (portable X-ray)
Documents & Manuals
No documents available for this device yet.
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