Varian Medical Systems · Model VariSource iX HDR afterloader
• Force feedback mechanism device helps ensure highest possible treatment success ratio • Smallest source in the industry (0.59mm dia. x 5mm long) permits use of needles as thin as 20 gauge and virtually eliminates catheter kinking • Ergonomically designed indexer enables precise connection of catheters to the afterloader • Internal CamScale system delivers accurate confirmation of wire position accuracy • Multiple safety & backup features (e.g., on-board radiation detector and emergency retract system)
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: Short runtime, low-battery alarm.
Root cause: Aged battery.
Symptoms: Intermittent signal/power.
Root cause: Repeated flexing.
Symptoms: Loose device, vibration damage.
Root cause: Docking latch wear.
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.
Critical for transport; spares mandatory.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Docking cradle / latch | Periodic replacement | $$ | Fairly easy |
| Patient cable set | Periodic replacement | $$ | Easy |
| Rechargeable battery pack Critical for transport; spares mandatory. | Frequent wear item | $$$ | Fairly easy |
Relative cost: $ lowest · $$$$ 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.
A defective treatment applicator in a cancer therapy medical device may become separated potentially causing patient injury.
Manufacturer of brachytherapy instrument issued a Customer Technical Bulletin to clarify instructions for use of the radiation treatment medical device by healthcare practitioners.
Radiation treatment software could potentially cause a healthcare practitioner to apply incorrect treatment regimen to patients undergoing brachytherapy.
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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