Teleflex Medical · Model ARROW InView Ultrasound
The Arrow InView Portable Ultrasound System puts high-quality imaging capabilities and simple controls.
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: Dropout, dead elements, image banding.
Root cause: Element delamination or cable damage from repeated use.
Symptoms: Intermittent image loss, connector-wiggle artifact.
Root cause: Repeated flexing and connector strain.
Symptoms: Frozen console, acquisition timeout.
Root cause: Workstation or storage degradation.
Symptoms: Dim image, color shift, dead pixels.
Root cause: Backlight or LCD panel 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.
Handle with care; most-replaced probe assembly.
| 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.
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.
Synced live from the FDA openFDA API.
The firm received reports indicating PTD tip separation during use.
The safety cap attached to needles within the needle sets may become dislodged exposing the needle and potentially causing the needle to protrude through the packaging. If this issue is not detected, the immediate risk of exposure to the affected devices is needle stick injury to the clinician or health care professional. In addition, a puncture of the packaging may compromise the sterility of the needle.
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
Sterility: Due to a potential incomplete seal on the outer sterile package.
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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