Aaron
Bovie DERM 101 and 102 Service Guide Rev 0
Service Guide
70 Pages
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SERVICE GUIDE
Service Guide • DERM 101/102
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This Service Guide and the equipment it describes are for qualified technicians who maintain and repair the Bovie® DERM 101/102 High Frequency Desiccator. Additional User information is available in the Bovie® DERM 101/102 User’s Guide. This document covers technical descriptions of the Bovie® DERM 101/102including its physical appearance, all operator controls and indications, operational specifications, component functional descriptions (module level), diagrams of the electronic circuits used, and troubleshooting guidelines (with chart comparisons). The Bovie DERM 101/102 was constructed with the highest quality components. In the unlikely event that your generator fails within two years of purchase date, Bovie Medical Corporation will warranty the product and effect factory repairs. Please refer to Appendix A, Warranty for what is covered, length of coverage, and “How to Receive a Return Authorization Number.”
Equipment Covered in this Manual Bovie DERM 101™, Bovie DERM 102™: Reference No.: DERM101, DERM102
For Information Contact Bovie Medical Corporation • 5115 Ulmerton Road, Clearwater, FL 33760 USA U.S. Phone 1-800-537-2790 Fax 1-800-323-1640 • International Phone +1-727-384-2323 Fax +1-727-347-9144 www.boviemed.com • [email protected]
DERM 101/102 Electrosurgical Desiccator: Reference No.: DERM 101, Reference No.: DERM 102 Manufactured by BovieBulgaria Ltd., Boul. Tsarigradsko shose No133, Building 3, fl.3 and fl.5, 1784 Sofia, Bulgaria, for Bovie Medical Corporation. ©2014 Bovie Medical Corporation. All rights reserved. Contents of this publication may not be reproduced without the written permission of Bovie Medical Corporation. Bovie Part Number MC-55-229-002 Rev. 0
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Bovie Medical Corporation
SAFETY PRECAUTIONS WHEN OPERATING THE GENERATOR The safe and effective use of electrosurgery depends to a large degree on factors solely under the control of the operator. There is no substitute for a properly trained and vigilant medical staff. It is important that they read, understand, and follow the operating instructions supplied with this electrosurgical equipment. To promote the safe use of the Bovie® DERM 101/102, please refer to the User’s Guide for standard operating precautions.
APPLICABLE SAFETY STANDARDS Conforms To ANSI/AAMI STD ES60601-1 IEC STD 60601-1-6 & 60101-2-2 Certified To CAN/CSA STD C22.2 No. 60601-1
CONVENTIONS USED IN THIS GUIDE WARNING: Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
CAUTION: Indicates a hazardous situation which, if not avoided, may result in minor or moderate injury.
NOTICE: Indicates an operating tip, a maintenance suggestion, or a hazard that may result in product damage.
Service Guide • DERM 101/102
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TABLE OF CONTENTS Equipment Covered in this Manual...ii For Information Contact ...ii Safety Precautions When Operating the Generator ...iii Applicable Safety Standards...iii Conventions Used in this Guide ...iii The Bovie DERM 101/102 ...1-1 Functional Description...1-2 Unit Description...1-2 Safety Precautions when Repairing the Generator...1-3 General Warnings, Cautions, and Notices ...1-3 Active Accessories ...1-3 Fire / Explosion Hazards ...1-4 Generator Electric Shock Hazards...1-4 Servicing...1-4 Cleaning ...1-4 Controls, Indicators and Receptacles...2-1 Front Panel...2-2 Controls and Indicators Overview ...2-3 Coagulation and Bipolar Controls ...2-4 Accessory Receptacles...2-5 Rear Panel View ...2-6 Front View on Wall Mount and Stand ...2-7 Side View Left and Right...2-8 Symbolson the Front and Rear Panels...2-9 Technical Specifications ...3-1 Performance Characteristics...3-1 Input Power ...3-1 Duty Cycle ...3-2 Dimensions and Weight ...3-2 Operating Parameters ...3-2 Transport ...3-2 Storage...3-2 Audio Volume ...3-2 Low Frequency (50-60 Hz) Leakage Current...3-3 High Frequency (RF) Leakage Current...3-3 Standards and IEC Classifications...3-3 Class I Equipment (IEC 60601-1) ...3-3 Type CF Equipment (IEC 60601-1) ...3-3 Drip Proof (IEC 60601-2-2) ...3-3 Electromagnetic Interference ...3-3 Electromagnetic Compatibility (IEC 60601-1-2 and IEC 60601-2-2) ...3-3 EMC Compliance ...3-4 Output Power Characteristics ...3-8 Maximum Output for Bipolar and Monopolar ...3-8
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Bovie Medical Corporation
Theory Of Operation ...4-1 Block Diagram...4-2 Functional Overview of Key Circuits ...4-2 System Logic...4-4 Bovie DERM 101/102 Control Signal Inputs and Outputs ...4-4 Operating the Bovie DERM 101/102 ...5-1 Inspecting the Generator and Accessories ...5-2 Service Personnel Safety...5-2 Installation and Placement ...5-3 Functional Checks...5-3 Unit Operations ...5-5 Maintenance...6-1 Cleaning ...6-2 Periodic Inspection...6-2 Fuse Replacement ...6-2 Troubleshooting ...7-1 Recommended Equipment for Troubleshooting...7-2 Troubleshooting the Bovie DERM 101/102...7-2 Inspecting the Generator...7-2 Inspecting the Receptacles ...7-2 Inspecting Internal Components...7-3 Understanding Error Codes and Audio Tones...7-4 Correcting Common Problems...7-5 Main Board Test Points ...7-8 Return Policy and Procedures...8-1 Responsibility of Manufacturer...8-2 Returning the Unit for Service...8-2 Warranty ...A-1 Board Drawings, Schematics, & Assemblies ...B-1 How to Order Parts from Bovie Medical Corporation ...B-2 Bovie DERM 101/102 Design Breakdown and Drawing Reference...B-2 Bovie® Drawing and Schematic Package ...B-3
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LIST OF FIGURES Figure 2 – 1 Figure 2 – 2 Figure 2 – 3 Figure 2 – 4 Figure 3 – 1 Figure 3 – 2 Figure 3 – 3 Figure 3 – 4 Figure 3 – 5 Figure 3 – 6 Figure 4 – 1 Figure 5 – 1 Figure 5 – 2 Figure 6 – 1
Layout of controls, indicators, and receptacles on the front panel...2-2 Controls for the cut, blend, and coag modes ...2-4 Location of the front panel receptacles and power switch ...2-5 Layout of controls and labeling on the rear panel...2-6 Output power versus power setting for all modes...3-8 Power setting versus voltage (Vpeak) for all modes...3-8 Output Power versus Load • Bipolar 100% / 50% ...3-9 Bipolar Mode waveform ...3-9 Output Power versus Load • Monopolar 100% / 50% ...3-10 Monopolar Mode waveform...3-10 Functional block diagram of the Bovie DERM 101/102 system...4-2 Installation and placement...5-3 Unit setup ...5-4 Fuse...6-2
SCHEMATICS AND BOARD DRAWINGS Main Board ...B-3 Logic Center ...B-4 RF Amplifier Circuit ...B-5 Activation Sense Circuit (Hand, Foot, Power Up and Power Down) ...B-6 Power Supply ...B-7 ADC Measurement Circuit ...B-8 AC/DC SMPS Power Supply...B-9 Audio (Buzzer) Control Circuit...B-10 Printed Circuit Board Main ...B-11 Bovie DERM 101/102 Assembly ...B-12
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Bovie Medical Corporation
THE BOVIE® DERM 101/102 HIGH FREQUENCY DESICCATOR This section includes the following information: ● Functional Description ● Unit Description ● Safety Precautions When Repairing the Generator ● General Warnings, Cautions, and Notices ● Active Accessories ● Fire/Explosion Hazards ● Generator Electric Shock Hazards ● Servicing ● Cleaning
CAUTION Read all warnings, cautions, and instructions provided with this generator before using. Read the instructions, warnings, and cautions provided with electrosurgical accessories before using. Specific instructions are not included in this manual.
Service Guide • DERM 101/102
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FUNCTIONAL DESCRIPTION The Bovie® DERM 101/102 is a multipurpose High Frequency Desiccator for use in physician’s offices and surgi-centers. It provides unsurpassed performance, flexibility, reliability, and user convenience in one compact package. TheBovie® DERM 101/102 High Frequency Desiccator includes digital technology. This new technology is evident in the self-checking circuitry and error code readouts. The DERM 101™ unit offers monopolar electrosurgical operations. The DERM 102™ unit offers monopolar and bipolar electrosurgical operations.
The following are key advantages and benefits. Power Capabilities
Up to 10 watts of Coagulation @ 1000 Ω. Up to 10 watts of Bipolar @ 150 Ω.
Memory
The generator automatically powers up to the last power setting.
Self Diagnostics
These diagnostics continually monitor the unit to ensure proper performance. Whenever they detect a problem, medical personnel receive audible and visual alarm responses, and the output is suspended until the alarm condition is cleared.
UNIT DESCRIPTION TheBovie® DERM 101/102 High Frequency Desiccator is a self-contained unit, consisting of the main enclosure and power cord. The main components incorporated in the generator include: • FRONT PANEL COMPONENTS Dial for controlling power output; receptacles for connecting electrosurgical accessories; footswitch receptacle; and 7-segment display. • REAR PANEL COMPONENTS Volume control. • OTHER COMPONENTS Power switch (located on side of unit); power cable receptacle (located on bottom of unit); connector to A902 pencil. • INTERNAL COMPONENTS Main PCB
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Bovie Medical Corporation
SAFETY PRECAUTIONS WHEN REPAIRING THE GENERATOR Before servicing the Bovie® DERM 101/102 High Frequency Desiccator it is important that you read, understand, and follow the instructions supplied with it. Also, be familiar with any other equipment used to install, test, adjust, or repair this generator.
General Warnings, Cautions, and Notices WARNING The instrument receptacles on this generator are designed to accept only one instrument at a time. Do not attempt to connect more than one instrument at a time into a given receptacle. Doing so will cause simultaneous activation of the instruments. To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective earth.
CAUTIONS 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. Unit is designed to be wall mounted or mounted on a mobile stand. Provide as much distance as possible between the electrosurgical generator and other electronic equipment (such as monitors). An activated electrosurgical generator may cause electrical interference with them. Do not turn the activation tone down to an inaudible level. The activation tone alerts the surgical team when an accessory is active. No modification of this equipment is allowed.
NOTICE Connect the power cord to a wall receptacle having the correct voltage. Otherwise, product damage may result.
Active Accessories WARNINGS Shock Hazard – Do not connect wet accessories to the generator. Shock Hazard – Ensure that all accessories and adapters are correctly connected and that no metal is exposed. Associated equipment and active accessories should be selected that have a rated accessory voltage equal to or greater than the maximum output voltage. Accessories must be connected to the proper receptacle type. In particular, bipolar accessories must be connected to the Bipolar Instrument output jack only. Improper connection may result in inadvertent generator activation.
CAUTIONS Accessories must be connected to the proper receptacle type. In particular, bipolar accessories must be connected to the Bipolar Instrument receptacle only. Improper connection may result in inadvertent generator 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. Refer to the accessories instructions for use for more detailed instructions. Set power levels to the lowest setting before testing an accessory.
Service Guide • DERM 101/102
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NOTICES To avoid incompatibility and unsafe operation, we recommend using only Bovie®/Aaron® accessories. During bipolar electrosurgery, do not activate the generator until the forceps have made contact with the patient. Product damage may occur.
Fire / Explosion Hazards WARNINGS Explosion Hazard – Do not install the generator in the presence of flammable anesthetics, gases, liquids, or objects. Fire Hazard – Do not place active accessories near or in contact with flammable materials (such as gauze or surgical drapes). Electrosurgical accessories that are activated or hot from use can cause a fire. Use a holster to hold electrosurgical accessories safely away from personnel and flammable materials. Fire Hazard – Do not use extension cords. Fire Hazard – For continued protection against fire hazard, replace fuses only with fuses of the same type and rating as the original fuse.
Generator Electric Shock Hazards WARNINGS Connect the generator power cord to a properly grounded receptacle. Do not use power plug adapters. To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective earth. Connect the power cord to a properly polarized and grounded power source with the frequency and voltage characteristics that match those listed on the back of the unit. Disconnect power cord from power source to isolate the internal circuits from the supply mains. Do not connect a wet power cord to the generator or to the wall receptacle. To allow stored energy to dissipate after power is disconnected (caps discharge) wait at least five minutes before replacing parts. Always turn off and unplug the generator before cleaning. Do not touch any exposed wiring or conductive surfaces while the generator is disassembled and energized. Never wear a grounding strap when working on an energized generator. When taking troubleshooting measurements use appropriate precautions such as using isolated tools and equipment, using the “one hand rule,” etc. Potentially lethal AC and DC voltages are present in the AC line circuitry, high voltage DC circuitry, and associated mounting and heat sink hardware described in this manual. These potentials are not isolated from the AC line. Take appropriate precautions when testing and troubleshooting this area of the generator. High frequency, high voltage signals that can cause severe burns are present in the RF output stage and in the associated mounting and heat sink hardware. Take appropriate precautions when testing and troubleshooting this area of the generator.
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Bovie Medical Corporation
Servicing CAUTIONS Read all warnings, cautions, and instructions provided with this generator before servicing. The generator contains electrostatic-sensitive components. When repairing the generator, work at a static-control workstation. Wear a grounding strap when handling electrostatic-sensitive components, except when working on an energized generator. Handle circuit boards by their nonconductive edges. Use an anti-static container for transport of electrostatic-sensitive components and circuit boards.
Cleaning NOTICE Do not clean the generator with abrasive cleaning or disinfectant compounds, solvents, or other materials that could scratch the panels or damage the generator.
Service Guide • DERM 101/102
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Bovie Medical Corporation
CONTROLS, INDICATORS, AND RECEPTACLES This section describes the front, rear, and side panels, including all controls, indicators, receptacles, and ports.
Service Guide • DERM 101/102
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FRONT PANEL Figure 2 – 1 Layout of controls, indicators, and receptacles on the front panel - DERM 101™
Figure 2 – 2 Layout of controls, indicators, and receptacles on the front panel- DERM 102™
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Bovie Medical Corporation
CONTROLS AND INDICATORS OVERVIEW Users may control most Bovie® DERM 101/102 functions from the front panel. Each Control is plainly marked on the front panel for quick reference. The volume control is located on the rear panel. Normal operations involve activating the generator with either a front connected handswitch or footswitch. The following components are the User Interface for the Bovie® DERM 101/102 High Frequency Desiccator: Power Switch
The rocker ON/OFF switch on the lower right corner. The switch turns power on and off to the unit.
Power Control Knob
This rotary knob allows you to select the desired RF power level for all modes of operation. The Power Control Knob moves at a graduated .1 watt per notch (incrementally) up to 10 watts.
Watts Display
The large power output display reports the generator’s output power setting from .1 to 10 watts.
Visual LED Indictors
The blue activation indicator reports when the unit is activated.
Audible Indicators
An activation tone sounds whenever the Bovie® DERM 101/102 High Frequency Desiccator is activated. The volume may be adjusted to a high or low setting. The volume adjust ment is located on the rear of the unit. An alarm siren sounds during all alarm conditions. The volume of this alarm cannot be adjusted.
Service Guide • DERM 101/102
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COAGULATION AND BIPOLAR CONTROLS Figure 2 – 3 Controls for the coag and bipolar modes
Coag and Bipolar Activation Indicator Illuminates when you activate Coag or Bipolar.
Coag and Bipolar Power Display (watts) Indicates the power set for Coag or Bipolar.
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Coag and Bipolar Power Control Dial Increases or decreases the Coag or Bipolar power output.
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ACCESSORY RECEPTACLES Figure 2 – 4 Location of the front panel receptacles and power switch
Power Switch Powers the unit on or off.
Handpiece Holder Securely holds Bovie® handpiece when not in use.
Monopolar Handswitching Receptacle Accepts only Bovie handpieces.
Patient Return Electrode Receptacle Accepts only Bovie return electrode plugs designed for the DERM 101/102.
Service Guide • DERM 101/102
Bipolar Receptacle Accepts only Bovie cables for bipolar handpieces.
Footswitching Receptacle Accepts only Bovie footswitch.
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REAR PANEL VIEW Figure 2 – 5 Layout of controls and labeling on the rear panel
Figure 2 – 6 Rear view mounted on stand
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Bovie Medical Corporation
FRONT VIEW ON WALL MOUNT AND STAND Figure 2 – 7 Front view on wall mount
Figure 2 – 8 Front view on stand
SIDE VIEW LEFT AND RIGHT Figure 2 – 9 Side view right (On/Off switch and power control knob)
Figure 2 – 10
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Side view left (pencil holster)
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