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WARNINGS:

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.

CAUTIONS:

At no time should you touch the active electrode or bipolar forceps. A burn could result.

Do not stack equipment on top of the generator or place the generator on top of electrical 
equipment. These configurations are unstable and/or do not allow adequate cooling.

Provide as much distance as possible between the electrosurgical generator and other electronic
equipment (such as monitors). An activated electrosurgical generator may cause interference 
with them.

Non-function of the generator may cause interruption of surgery. A backup generator should be
available for use.

Do not turn the activation tone down to an inaudible level. The activation tone alerts the surgical
team when an accessory is active.

When using a smoke evacuator in conjunction with the electrosurgical generator, place the smoke
evacuator a distance from the generator and set the generator volume control at a level that
ensures that the activation tones can be heard.

The use of high frequency 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, place any monitoring electrodes as far as possible from 
the surgical electrodes. Monitoring systems incorporating high frequency current-limiting devices
are recommended.

Do not use needles as monitoring electrodes during electrosurgical procedures. Inadvertent 
electrosurgical burns may result.

To avoid the possibility of a burn to the patient, when using a split pad do not activate the unit if
the solid pad indicator is illuminated green or the red alarm indicator remains illuminated red. This
could indicate improper pad placement or a faulty NEM circuit.

To avoid the possibility of an electrosurgical burn to either the patient or the physicians, do 
not allow the patient to come in contact with a grounded metal object during activation. When 
activating the unit, do not allow direct skin contact between the patient and the physician. 

The patient should not come in contact with metal parts which are earthed or which have an
appreciable capacitance to earth (for example operating table supports, etc.). The use of antistatic
sheeting is recommended for this purpose.

Remove any loose fitting jewelry from the patient before activation.

Examine all accessories and connections to the electrosurgical generator before use. Ensure that
the accessories function as intended. Improper connection may result in arcs, sparks, accessory
malfunction, or unintended surgical effects.

When not using active accessories, place them in a holster or in a clean, dry, non-conductive, and
highly visible area not in contact with the patient. Inadvertent contact with the patient may result 
in burns.

Avoid HF output settings where maximum output voltage may exceed rated accessory voltage.
Refer to the accessory’s voltage rating. Choose only accessories that will withstand each mode
and power setting.

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Bovie Medical Corporation

Содержание ids-400

Страница 1: ......

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

Страница 3: ...ii Bovie Medical Corporation...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

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

Страница 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...

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

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

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

Страница 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...

Страница 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...

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

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

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

Страница 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...

Страница 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...

Страница 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...

Страница 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...

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

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

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

Страница 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...

Страница 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...

Страница 64: ......

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