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RESPONSIBILITY OF THE MANUFACTURER

Bovie Medical Corporation is responsible for the safety, reliability, and performance of the generator only under the following 
circumstances:

• The user has followed the Installation and Setup Procedures in this User’s Guide.
• Persons authorized by Bovie Medical Corporation performed assembly operation, readjustments, modifications, or repairs.
• The electrical installation of the relevant room complies with local codes and regulatory requirements, such as IEC and BSI.
• Equipment use is in accordance with the Bovie Medical Corporation instructions for use.
• Equipment to be diposed/recycled.

Please note that infected medical devices must be disposed of as medical/biohazard waste and cannot be included in used 
electronic equipment disposal/recycling programs. In addition, certain electronic products must be returned directly to Bovie
Medical Corporation. Contact your Bovie Medical Corporation representative for return instructions.

For warranty information, refer to Appendix B

- Warranty

.

RETURNING THE UNIT FOR SERVICE

Before you return the unit, call your Bovie Medical Corporation representative for assistance. If instructed to send the unit to Bovie
Medical Corporation, first obtain a Returned Goods Authorization Number.  Then, clean the Unit and package securely to ensure
proper protection of the unit. So as to aid in the processing of the unit, please be sure to include a reference to the Bovie Return
Goods Authorization Number on the outside of the box and ship directly to Bovie Medical Corporation.

Step 1 – Obtain a Returned Goods Authorization Number

Call the Bovie Medical Corporation Customer Service Center (727) 384-2323 to obtain a Returned Goods Authorization Number.
Have the following information ready when you call:

• Hospital / clinic name / customer number

• Description of the problem

• Telephone number/fax number

• Type of repair to be done

• Department / address, city, state, and zip code

• P.O. number

• Model number / Serial number

Step 2 – Clean the Unit

WARNING:

Electric Shock Hazard

- Always turn off and unplug the unit before cleaning.

The use of flammable anesthetics or oxidizing gases such as nitrous oxide (N2O) and oxygen

should be avoided if a surgical procedure is carried out in the region of the thorax or the head,
unless these agents are sucked away.

Non-flammable agents should be used for cleaning and disinfection wherever possible.

Flammable agents used for cleaning or disinfecting, or as solvents of adhesives, should be
allowed to evaporate before the application if HF surgery. There is a risk of pooling flammable
solutions under the patient or in body depressions such as the umbilicus, and in body cavities
such as the vagina. Any fluids pooled in these areas should be mopped up before HF surgical
equipment is used. Attention should be called to the danger of ignition of endogenous gases.
Some materials, for example cotton, wool and gauze, when saturated with oxygen may be ignited
by sparks produced in Normal Use of the HF surgical equipment.

NOTICE:

Do not clean the unit with abrasive cleaning or disinfectant compounds, solvents, or other materi-
als that could scratch the panels or damage the unit.

7-2

Bovie Medical Corporation

Summary of Contents for ids-400

Page 1: ......

Page 2: ...i User s Guide Bovie IDS 400 USER S GUIDE...

Page 3: ...ii Bovie Medical Corporation...

Page 4: ...7 2790 Fax 1 800 323 1640 International Phone 1 727 384 2323 Fax 1 727 347 9144 www boviemed com info boviemed com 2014 Bovie Medical Corporation All rights reserved Contents of this publication may n...

Page 5: ...cks 3 2 Setting Up the Unit 3 2 Checking the Return Electrode Alarm 3 2 Confirming Modes 3 3 Checking Bipolar Mode with bipolar footswitch 3 3 Checking Monopolar Mode with monopolar footswitch 3 3 Che...

Page 6: ...age A 2 Audio Volume A 3 Return Electrode Sensing A 3 Low Frequency 50 60 Hz Leakage Current A 3 High Frequency RF Leakage Current A 4 Standards and IEC Classifications A 4 Class I Equipment IEC 60601...

Page 7: ...the unit power switch and front panel receptacles 2 9 Figure 2 8 Layout of connectors and controls on the rear panel 2 10 Figure 5 1 Fuse holder 5 2 Figure A 1 Output power versus voltage for all mod...

Page 8: ...y Warnings and Cautions Key Features Components and Accessories Additional Accessories CAUTIONS Read all warnings cautions and instructions provided with this generator before using Read the instructi...

Page 9: ...he bowel Oxygen enriched atmospheres Oxidizing agents such as nitrous oxide N20 atmospheres The sparking and heating associated with electrosurgery can provide an ignition source Observe fire precauti...

Page 10: ...tal resistance is within the preset safety range Proper application and visual inspection of the patient return electrode is required for safe operation In some circumstances potential exists for alte...

Page 11: ...etic equipment When high frequency surgical equipment and physiological monitoring equipment are used simultaneously on the same patient place any monitoring electrodes as far as possible from the sur...

Page 12: ...ces National Institute for Occupational Safety and Health NIOSH Control of Smoke from Laser Electric Surgical Procedures HAZARD CONTROLS Publication No 96 128 September 1996 Contraindications There ar...

Page 13: ...ediately adjusts the power to varying impedance during the electrosurgical procedure The unit s digital technology senses and responds to changes in tissue and density Unlike analog this feature reduc...

Page 14: ...for connecting footswitching pencil A905EL adaptor for 1 6 electrode into 3 32 collet BV 1253B footswitch for Monopolar procedures BV 1254B footswitch for Bipolar and vessel sealing procedures A827 fo...

Page 15: ...1 8 Bovie Medical Corporation...

Page 16: ...2 1 User s Guide Bovie IDS 400 CONTROLS INDICATORS AND RECEPTACLES This section describes The Front and Rear Panels Controls Indicators Receptacles and Ports...

Page 17: ...FRONT PANEL Figure 2 1 Layout of controls indicators and receptacles on the front panel 2 2 Bovie Medical Corporation...

Page 18: ...pray Mode Bipolar Controls Bipolar Mode Indicators Split Return Electrode Solid Return Electrode Regulatory Symbology Read instructions before use Defibrillator Proof Type CF Equipment RF Isolated pat...

Page 19: ...the 10 user defined presets Press and hold the Set button for three seconds to save the settings Recall Button Toggles through the 10 presets Stop at the desired number 0 9 illuminated in the Preset...

Page 20: ...tween Cut I Cut II and Blend modes Blend Amount Indicator Indicates the amount of blend added in the Blend mode More bars illuminated indicates more blend divided into 10 steps Blend Amount Control Bu...

Page 21: ...ns Increases or decreases the Pinpoint or Spray Coag power output in increments of 1 to 10 watts Coag Activation Indicator Illuminates when Coag mode is activated Pinpoint and Spray Mode Selector Togg...

Page 22: ...lar Power Display watts Indicates the power set for the Bipolar mode Displays error code in the event of an error Bipolar Power Control Buttons Increases or decreases the Bipolar power output in incre...

Page 23: ...en when the system detects a single plate Notices Solid pad indicator only detects that a pad is connected to the unit The unit does not moni tor pad placement on the patient Split Return Electrode In...

Page 24: ...Footswitching Receptacle Accepts cables or adapters equipped with standard active plugs Connect footswitching accessories Bipolar Receptacle Accepts standard cables for bipolar handpieces Connect bipo...

Page 25: ...ces must be disposed of as medical biohazard waste and 2 10 Bovie Medical Corporation SYMBOLS DESCRIPTION Equipotential Ground Stud Non ionizing Radiation Volume Control Danger Explosion Risk If Used...

Page 26: ...3 1 User s Guide Bovie IDS 400 GETTING STARTED This section includes the following information Initial Inspection Installation Function Checks Performance Checks...

Page 27: ...connectors and controls WARNING At no time should you touch the active electrode or bipolar forceps A burn could result Setting Up the Unit 1 Verify that the Power Switch is in the Off O position and...

Page 28: ...erates the Cut activation tone 4 While activating the Cut mode rotate the volume control over the full range to verify that the sound is audible throughout the range 5 Press the Coag pedal blue on the...

Page 29: ...3 4 Bovie Medical Corporation...

Page 30: ...ng for Monopolar Surgery Preparing for Bipolar Surgery Setting and Recalling Memory Presets Activating the Unit Activation Safety CAUTIONS Read all warnings cautions and instructions provided with thi...

Page 31: ...serious unintended patient injury including bowel perforation and unintended irreversible tissue necrosis For surgical procedures where the high frequency current could flow through parts of the body...

Page 32: ...heels are recommended For details refer to the procedures for your institution or to local codes Provide at least 10 to 15 cm 4 to 6 in of space from the sides and top of the generator for cooling Nor...

Page 33: ...tor the resistance at the contact between the electrode and the patient 2 Adjust the Blend setting to the desired amount of hemostasis Level 1 10 Adjustment is preformed by pressing the up or down but...

Page 34: ...ing activation Recall and Set membrane switches are disabled during activation During activation the activated mode can be adjusted up and or down a maximum of four steps Refer to the following table...

Page 35: ...allows the unit to display the last selected power preset when the generator is turned on NOTICE To have a setting selection available at startup or to be one of the 10 user defined presets the adjus...

Page 36: ...will be displayed and available when the unit is activated The number 2 Preset will now be the last saved Preset settings for Preset 2 ACTIVATING THE UNIT NOTICE Review Activation Safety on page 6 of...

Page 37: ...y current can interfere with the function of other electromagnetic equipment When high frequency surgical equipment and physiological monitoring equipment are used simultaneously on the same patient p...

Page 38: ...5 1 User s Guide Bovie IDS 400 MAINTAINING THE BOVIE IDS 400 This section covers the following topics Cleaning Periodic Inspection Fuse Replacement...

Page 39: ...uids to enter the chassis Do not sterilize the generator PERIODIC INSPECTION Every six months visually inspect the Bovie IDS 400 for signs of wear or damage In particular look for any of the following...

Page 40: ...6 1 User s Guide Bovie IDS 400 TROUBLESHOOTING This section includes Error Code Descriptions and actions to take to resolve them...

Page 41: ...tswitch pedal may be stuck F6 Simultaneous activation error The unit does not allow simultaneous activation of the cut and coagulation modes The activation mode is first come first serve This means th...

Page 42: ...7 1 User s Guide Bovie IDS 400 REPAIR POLICY AND PROCEDURES Refer to this section for information on Responsibility of the Manufacturer Returning the Generator for Service...

Page 43: ...x and ship directly to Bovie Medical Corporation Step 1 Obtain a Returned Goods Authorization Number Call the Bovie Medical Corporation Customer Service Center 727 384 2323 to obtain a Returned Goods...

Page 44: ...umber and the information hospital phone number etc listed in Step 1 Obtain a Returned Goods Authorization Number B Be sure the unit is completely dry before you pack it for shipment Although the pref...

Page 45: ...7 4 Bovie Medical Corporation...

Page 46: ...0 TECHNICAL SPECIFICATIONS All specifications are nominal and subject to change without notice A specification referred to as typical is within 20 of a stated value at room temperature 25 C 77 F and a...

Page 47: ...e device should be stored and used in a room temperature of approximately 770 F 250 C A 2 Bovie Medical Corporation Ambient temperature range 40 to 70 C Relative humidity 10 to 100 including condensat...

Page 48: ...not adjustable 70 dB 5 dB Frequency 2 kHz 1 2 seconds 1 kHz 1 2 seconds Duration 2 seconds Solid Trip resistance 0 to 5 3 Continuous measurement Once the system establishes the solid return electrode...

Page 49: ...wet electrical insulation or other components which when wet are likely to affect adversely the safety of the generator Electromagnetic Interference When other equipment is placed on or beneath a Bovi...

Page 50: ...IDS 400 The IDS 400 and its accessories are not suitable for interconnection with other equipment Portable and mobile RF communications equipment can affect Medical Electrical Equipment The IDS 400 sh...

Page 51: ...quency of the transmitter where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE 1 At 80 MHz and 800 MHz the separation distance for th...

Page 52: ...V differential mode 2 kV common mode 1 kV differential mode 2 kV common Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interruptions and voltage...

Page 53: ...the compliance level in each frequency range b Interference may occur in the vicinity of equipment marked with the following symbol NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher...

Page 54: ...ustrate specific output power delivered to a range of load resistances for each mode Figures A 9 through A 14 illustrate outpput power curves that depict the changes for each mode at specific power se...

Page 55: ...Bovie Medical Corporation A 10 Figure A 3 Output power versus impedance for Cut II mode Figure A 4 Output power versus impedance for Blend Min mode...

Page 56: ...User s Guide Bovie IDS 400 A 11 Figure A 5 Output power vs impedance for Blend Max mode Figure A 6 Output power vs impedance for Pinpoint mode...

Page 57: ...Figure A 7 Output power vs impedance for Spray mode Figure A 8 Output power vs impedance for Bipolar mode A 12 Bovie Medical Corporation...

Page 58: ...Figure A 9 Power setting versus output power for Cut I mode Figure A 10 Power setting versus output power for Cut II mode A 13 User s Guide Bovie IDS 400...

Page 59: ...Figure A 11 Power setting versus output power for Blend Min and Max mode Figure A 12 Power setting versus output power for Pinpoint mode A 14 Bovie Medical Corporation...

Page 60: ...Figure A 13 Power setting versus output power for Spray mode Figure A 14 Power setting versus output power for Bipolar mode A 15 User s Guide Bovie IDS 400...

Page 61: ...A 16 Bovie Medical Corporation...

Page 62: ...ch has been repaired or altered outside Bovie s factory in a way so as in Bovie s judgment to affect its stability or reliability or which has been subjected to misuse neglect or accident The warranty...

Page 63: ...any liability hereunder or elsewhere in connection with the sale of this product for indirect or consequential damages This warranty and the rights and obligations hereunder shall be construed under a...

Page 64: ......

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