
AngioDynamics · Model Venacure 1470
Quality craftsmanship and high performance design. Intuitive controls and interconnects for ease of use. The Fiber Recognition System (FRS) which programs the laser for the specific fiber type being used, allowing for fewer steps and shorter procedure time Fiber Recognition System (FRS). Faster procedure set-up with preset parameters. Immediate recognition of procedure presets. Protective door helps prevent dust particles from damaging laser or fiber Quality. Industry-leading 3-year standard warranty ensures every laser will receive top-notch service. Internal sensors constantly monitor wattage ensuring a constant energy output. More than 20 safety features at and above standard Easy to Use. Intuitive user interface with fewer buttons. Programmable sound pulses allows for audible tracking of pull-back rate which increases repeatability of treatment. Aiming beam with variable modes and brightness increases visibility in patient. Real-time on-screen display of treatment energy. Lightweight, Compact and Portable. Easily transported between hospital and office MultiMedia Card (MMC). Stores data for at least 100 treatments. Automated tracking of procedure and fiber records. Available USB-MMC (SD memory card) card reader/writer enables easy data transfer to PC.
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.
Symptoms: Weak or no output at the delivery device, treatment ineffective, power not reaching the set value.
Root cause: Laser module / lamp / diode-bar ageing, a damaged delivery fibre / handpiece / applicator, or a driver / power-supply fault.
Symptoms: Unit shuts down after a period, over-temperature or low-flow alarm.
Root cause: Chiller / TEC fault, low or contaminated coolant, a failed pump, or blocked airflow.
Symptoms: Burn marks at the tip, high loss, intermittent output, applicator not recognised.
Root cause: Damaged or contaminated fibre / applicator / connector.
Symptoms: Skin cooling not delivered, cooling / cryogen alarm.
Root cause: Contact-cooling / cryogen supply, a valve, or the tip.
Symptoms: Laser will not fire, key / interlock / footswitch error.
Root cause: Footswitch, door interlock, or key-switch fault.
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.
Power re-calibration required after replacement.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Laser module / lamp / diode bar Power re-calibration required after replacement. | Periodic replacement | $$$$ | Expert-level |
| Delivery fibre / handpiece / applicator | Frequent wear item | $$$ | Fairly easy |
| Chiller / TEC components & coolant filter | Periodic replacement | $$$ | Difficult |
| Contact-cooling tip / cryogen valve (aesthetic) | Periodic replacement | $$ | Moderate |
| Footswitch | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ 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 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.
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.
OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not meet the required dimensional specification, may result in damage to the sheath, including separation or the inability to move the fiber within the sheath. A damaged sheath will necessitate removal from the patient, which may result in procedural delay and/or surgical intervention
The affected product is properly labelled with an expiration date of March 31, 2022; but the RFID programmed expiration date is April-2014 which results in an error message when connected to the laser source and prevents the product from being used.
AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT NeverTouch Procedure Kits, because the potential exists that the micro Introducer (sheath/dilator) packaged within the kit could be the wrong French size.
During an in-process inspection the hemostasis sidearm assemblies were identified to have the potential for flash to exist on the housing at the base of the threads. This flash has the potential to break off and relocate within the fluid path.
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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