AngioDynamics RITA® Model 1500X RF generator
AngioDynamics · Model RITA® Model 1500X RF generator
New Habib mode. Remote foot pedal control. Automated ablation algorithm. Expanded memory capacity. Fully-automated generator recognizes which device is plugged in and will automatically load the proper protocol.
Key tips
- ·Never defeat or bypass a return-electrode monitoring (REM) alarm to finish a case - it's a direct burn risk.
- ·Verify OR table battery backup - a table that loses power mid-procedure is a real, documented incident type.
- ·Track surgical light lamp-hours rather than waiting for failure - a sudden failure mid-case is avoidable.
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.
No or low RF output / high-impedance cut-out
HighSymptoms: No cut / coag effect, "high impedance" or output-error message, output shuts down.
Root cause: Poor electrode contact or a dry field, a damaged handpiece / cable, a return-electrode (REM/NESSY) fault, or an output-stage fault.
Return-electrode (patient-plate) contact-quality alarm
MediumSymptoms: REM / NESSY / plate alarm, monopolar output inhibited.
Root cause: Poorly applied or dried split dispersive pad, a pad-cable fault, or the contact-quality-monitor circuit.
Bipolar / vessel-sealing output fault
MediumSymptoms: Bipolar or sealing output weak, seal cycle will not complete, instrument not recognised.
Root cause: Bipolar cable / instrument fault or the sealing output stage.
Fails calibration / output drifts after a repair
MediumSymptoms: Output power or the REM circuit outside tolerance on the analyser.
Root cause: Output board or REM circuit needs recalibration - anti-static handling required.
Footswitch / handswitch fault
MediumSymptoms: Output will not activate from the pedal or the handpiece.
Root cause: Footswitch or handswitch / cable fault.
Touchscreen / display / boot fault
LowSymptoms: Unresponsive touchscreen, will not power on or boot, fan / thermal alarm.
Root cause: Display, power supply, control board, or a cooling-fan fault.
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.
Reusable instrument / handpiece cables
Class Periodic replacementRel. cost $$R&R Easy
Split dispersive (return) pads
Class ConsumableRel. cost $R&R Easy
Footswitch
Class Periodic replacementRel. cost $$R&R Fairly easy
Bipolar / sealing cable
Class Periodic replacementRel. cost $$R&R Easy
RF output board
Recalibration required after replacement; anti-static handling.
Class Major service partRel. cost $$$$R&R Difficult
Cooling fan
Class Major service partRel. cost $R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Reusable instrument / handpiece cables | Periodic replacement | $$ | Easy |
| Split dispersive (return) pads | Consumable | $ | Easy |
| Footswitch | Periodic replacement | $$ | Fairly easy |
| Bipolar / sealing cable | Periodic replacement | $$ | Easy |
| RF output board Recalibration required after replacement; anti-static handling. | Major service part | $$$$ | Difficult |
| Cooling fan | Major service part | $ | Moderate |
Relative cost: $ lowest · $$$$ 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.
- ·Pre-case functional check
- ·Electrosurgical return-electrode cable inspection
- ·Table hydraulic / mechanical inspection
- ·Annual electrical safety test and full PM
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: No or low RF output / high-impedance cut-out
- Confirm good electrode-tissue contact and an adequately wetted field.
- Inspect the handpiece / instrument and its cable for damage; substitute a known-good one.
- Check the split dispersive (return) pad is well applied over well-perfused muscle with a sound cable.
- Verify output into a resistive test load with an electrosurgical analyser.
- Replace the RF output board and recalibrate on a non-conductive surface if output is confirmed absent (anti-static handling).
Symptom: Return-electrode (REM / NESSY / CQM) contact-quality alarm
- Re-apply a fresh split dispersive pad with full skin contact.
- Check the pad cable and its connector.
- Try a known-good pad.
- Run the contact-quality-monitor calibration with a good pad fitted.
- Refer the CQM circuit if it still alarms.
Symptom: Output will not activate from the footswitch or handswitch
- Test the other activation method to isolate the pedal from the handpiece.
- Inspect the footswitch and its cable / connector for damage or moisture.
- Check the handswitch leads on the handpiece.
- Substitute a known-good footswitch.
- Refer the activation input board if both methods fail.
Symptom: Fails calibration / output drifts after a repair
- Verify cut and coag output at several settings into a test load with an analyser.
- Verify the REM / CQM circuit against its spec.
- Recalibrate per the service manual on a non-conductive bench with anti-static precautions.
- Check the cooling fan and thermal path.
- Re-verify all outputs and the REM alarm before returning to service.
Technical Specs
- Height
- 13.5 cm
- Length
- 43 cm
- Weight
- 23 lbs
- OutPut Frequency
- 460 kHz ±5%
- Output Power
- 100 V - 240 V, 50 - 60 Hz, Auto-Switching Power Supply
- Width
- 37.5 cm
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Operating rooms
- Procedure rooms
- Interventional suites
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
- RECALL
Updated Warning Statements in the Operator's Manual/Directions for Use and Software Updates to reduce the risk of potential patient harm due to a delay in performing a procedure
- RECALL
The firm is recalling product that has the potential to not function during use. The product affected by this recall will not deliver the desired microwave energy due to coolant ingress in an electrical connection; this condition results in an error code High Reflective Power displayed on the microwave generator.
- RECALL
The RITA Main Cable product contains the incorrect Instructions for Use.
- RECALL
Angiodynamics was marketing the NanoKnife System with the ablation zone estimator feature in the US without FDA clearance.
- RECALL
Some units of Nanoknife have the potential to deliver a shortened pulse width without indicating an error. The affected units contain a "GOMe" circuit board which may cause the generator to drift from the calibration points set at the time of manufacture.
- RECALL
The labeling contains errors which result in the products being misbranded
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