AtriCure nContact CS-3000 Operator'S Manual Download Page 8

CS-3000 RF Generator Unit Operator Manual

AtriCure, Inc.

IFU-0022.A

2021/04

Page 8 / 12

CSK Type Devices, CSK-2000 Cable and RF Generator Setup

Refer to the drawing below for the appropriate setup of the CSK devices with the 

CSK-2000 cable and the CS-3000 generator.

Figure 5.  CSK Type Devices, CSK-2000 Cable and RF Generator Setup

CDK Type Devices, CSK-2030, CSK-2000 Cable and RF Generator Setup

Refer to the drawing below for the appropriate setup of the CDK devices with the 

CSK-2000 cable, CSK-2030 cable and the CS-3000 generator.

Figure 6A.  CDK Type Devices, CSK-2000, CSK-2030 with over molded 

yoke and RF Generator Setup

Figure 6B.  CDK Type Devices, CSK-2000, CSK-2030 with enclosure 

box and RF Generator Setup

D1 = Distal Electrode 1 = Shrouded Pin #1;    P1 = Proximal Electrode 1 = Shrouded Pin #3; 

D2 =

 

Distal Electrode 2 = Shrouded Pin #2;    P2 =

 

Proximal Electrode 2 = Shrouded Pin #4

 

CAUTION

:  Ensure that the EP Sensing (EKG) equipment comply with IEC 

60601-2-25 for protection from high frequency surgical interference.

Back Panel Connectors

Figure 7.  Generator Back Panel – Key Features

Power Switch (13)

Switch that powers the generator on and off.

AC Power Connector (14)

Connector for the AC line power cable.

Grounding Stud (15)

Used as a ground equalization for safety and testing.

Data Connector (16)

USB or Serial communication connector to a host computer for data display and 

archival purposes.

Alarm Volume Control (17)

Knob for modifying the volume of the generator alarm.  Rotate the knob clockwise to 

increase the volume.

Chapter 2 Setup and Operation

Generator Setup and Operation

Preparing the Patient – Attaching the Indifferent, Dispersive Electrode

Prepare the patient for electrosurgery following standard protocol.  Ensure patient’s 

entire body, including extremities, is insulated against contact with grounded metal 

parts.  Closely follow instructions for the coagulation device and manufacturer direc-

tions for the indifferent, dispersive electrode.

 CAUTION

:  Failure to achieve good skin contact by the entire adhesive surface 

of the indifferent, dispersive electrode could result in a patient burn or poor electrical 

performance from the coagulation device.  Note:  Patient Return Electrode (e.g. Indif-

ferent, Dispersive Electrode), surface area of 21 square inches (136cm

2

), equivalent 

to Covidien Valleylab

 

Polyhesive Reference Number E7506 is recommended.

Setting up the CS-3000 RF Generator

1.  Connect the supplied power cord into back mains receptacle of the CS-3000 

RF Generator.

2.  Plug the CS-3000 RF Generator power cord into an outlet.
3.  On the back of the CS-3000, activate the mains switch and turn the RF 

Generator on.

4.  Turning on the generator (switch on rear of generator) causes the system 

to enter Standby mode where no measurements or settings are possible.  

The nContact logo and the software version number are displayed in the 

message window; the Standby LED is illuminated.

5.  Press the Mode button to perform a self-test and check system functionality 

before transitioning to Power Control mode.  Subsequent depressing of the 

Mode button will toggle between Power Control and Diagnostic Evaluation 

modes.

NOTE

:  If an Error is detected, the red Error LED will illuminate

,

 and a Message 

will display in the Graphic Display.  Cycle the CS-3000 main power off and on so 

the RF Generator passes through self-test.  (see Chapter 6:  Troubleshooting).

CS-3000 Operation in Power Control Mode

When the RF Generator enters 

Power Control

 mode, the initial Power is set to 4 W 

and Time is set to 0 until a Coagulation Device is connected via the RF coagulation 

cable to the receptacle in the generator.  
Connect a coagulation device to the appropriate receptacle (blue) of the cable then 

connect the cable (black) to the receptacle on the RF generator so the pre-set Pow-

er and Time values are displayed. Refer to the instruction for use of the coagulation 

devices for the appropriate pre-set power and time settings.

Summary of Contents for nContact CS-3000

Page 1: ...restricts this device to sale by or on the order of a physician Disclaimer AtriCure reserves the right to change its products and services at any time to incorporate the latest technological developments This Manual is subject to change without notice Although this Manual has been prepared with every precaution to ensure accuracy AtriCure assumes no liability for damages resulting from the applica...

Page 2: ... and Operation 8 Generator Setup and Operation 8 Chapter 3 Cleaning 9 Chapter 4 Technical Specifications and Safety Inspection 9 Device Specifications 9 Environmental Specifications 9 Periodic Inspections 9 Chapter 5 Product Specifications 10 Operational Conditions Front Panel Displays 10 Figure 8 RF Generator Front Panel Display at Power On 10 Figure 9 RF Generator Front Panel Display at Standby ...

Page 3: ...connect to earthed ground Follow the manufacturer s directions for the placement of the indifferent dispersive electrode and for proper insulation between the patient and any metallic surfaces o Maintain safe handling techniques during electrocoagulation due to electric fields and hot metallic surfaces o Do not touch the electrode surface of the Coagulation Device and the Indifferent Dispersive El...

Page 4: ...ality should be that of a typical commercial or hospital environment Voltage Dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 Voltage Dips 0 Vt 0 5 cycle At 0 45 90 135 180 225 270 and 315 phase angles 0 Vt 1 cycle and 70 Vt 25 30 cycles Single phase at 0 Voltage interruptions 0 Vt 250 300 cycle Voltage Dips 0 Vt 0 5 cycle At 0 45 90 135 180 225 270 and 31...

Page 5: ...radiated RF disturbances are controlled The customer or the user of the CS 3000 RF Generator can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the CS 3000 RF Generator as recommended below according to the maximum output power of the communications equipment Rated Maximum Output Power of Transmit...

Page 6: ...e generator operates in either the Power Control or Diagnostic Evaluation mode When operating in Power Control mode set the desired duration and Power level The generator will transmit Power at the set point for the Time set by the operator Power may be adjusted manually throughout the treatment to tailor the coagulation process but caution should be used when deviating from the recom mended pre s...

Page 7: ...in impedance Impedance 5 Impedance resistance between the coagulation device and the indifferent dispersive electrode is measured by the generator and displayed in ohms Ω A bar graph shows the change in impedance between the initiation of RF energy baseline and throughout tissue coagulation test As conductivity decreases impedance increases During coagulation of tissue when the temperature of the ...

Page 8: ...e coagulation device and manufacturer direc tions for the indifferent dispersive electrode CAUTION Failure to achieve good skin contact by the entire adhesive surface of the indifferent dispersive electrode could result in a patient burn or poor electrical performance from the coagulation device Note Patient Return Electrode e g Indif ferent Dispersive Electrode surface area of 21 square inches 13...

Page 9: ...G Ensure Isopropyl Alcohol IPA is completely dry before oper ating the unit CAUTION Avoid caustic or abrasive cleaners Guidelines The following guidelines are recommended for cleaning the unit It is the user s responsibility to qualify any deviations from these processing methods 1 Disconnect the unit or cart from the outlet before cleaning 2 If the unit and or accessories are contaminated with bl...

Page 10: ...nd transmit RF energy to the coagulation device The RF ON OFF LED is activated Power is preset for the coagulation devices The cycle Time e g 56 s is displayed in lower right corner and counts up to the set value Impedance is measured and the value displayed in the lower left e g 105 Ω Impedance is graphed in the right Test bar against the baseline value mea sured at initiation of RF The baseline ...

Page 11: ...rected Once the warning is corrected then the parameters reset to the preset values Final Impedance 765 Ω is displayed and graphed against the baseline 100 Ω Final Percent change in impedance is displayed 665 Final Power transmitted shown 50 W Time at User Termination of RF energy 34 s displayed When this warning occurs an audible tone will sound three times for 1 5 seconds with 450 milliseconds b...

Page 12: ...ng the use of the nContact Coagulation system please contact Customer Service at AtriCure Incorporated 7555 Innovation Way Mason Ohio 45040 USA Customer Service 1 866 349 2342 toll free 1 513 755 4100 phone EC REP AtriCure Europe B V De Entree 260 1101 EE Amsterdam The Netherlands 31 20 7005560 ear atricure com WARRANTIES Limitation on Liability This warranty and the rights and obligations hereund...

Reviews: