Triton Dental Operative Unit - Model 2021 - ASI Dental
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Triton™ Dental Operative Unit - Model 2021 OPERATION and SERVICE MANUAL PN: 65-2021 | Rev. A This Operation and Service Manual includes sections for optional components that may or may not be included in your system. Your system may contain built-in accessory instruments from other manufacturers. Please refer to the original manufacturer’s instructions for operation and maintenance of those instruments. Advanced Dental Systems® & Advanced Endodontic Systems® 13792 Compark Blvd | Suite 130 | Englewood, CO 80112 | www.asimedical.net Main: (303) 766-3646 | Toll Free: (800) 566-9953 | Fax: (303) 565-8929 (Service Dept.)
Triton™ 2021 Manual 1.0 PRODUCT DESCRIPTION, INSTALLATION, AND SAFETY PRECAUTIONS.........4 1.1 Safety Precautions and Warnings.........................................................................................................4 1.2 Product Descriptions, Function and Intended Use...............................................................................5 1.3 Dimensional Specifications, Capacities and Technical Data...............................................................6 1.4 Operating Environment and Classification of Equipment....................................................................7 1.5 Unpacking and Setup..........................................................................................................................8 1.6 Voltage Selection.................................................................................................................................8 1.7 Electical...............................................................................................................................................8 1.8 Installation of the Optional Purge Hose Quick Connect Kit................................................................9 1.9 Optional Installation to Utility Center Systems.....................................................................................10 2.0 COMPONENT OPERATING INSTRUCTIONS..................................................11 2.1 Clean Closed Water System.................................................................................................................11 2.2 Air/Water Syringe.................................................................................................................................11 2.3 Handpiece...........................................................................................................................................12 2.4 Fiber Optics.........................................................................................................................................12 2.5 Oral Evacuation System.......................................................................................................................13 2.6 Self-Contained Vacuum Pump.............................................................................................................13 2.7 Suction Canister with Amalgam Separator..........................................................................................13 3.0 MAINTENANCE...........................................................................................14 3.1 Equipment Care and Inspection...........................................................................................................14 3.2 Purging the Waste Canister and Cleaning the Evacuation System......................................................14 3.3 Amalgam Separator Bowl Checking and Replacement.......................................................................15 3.4 System Air Pressure..............................................................................................................................15 3.5 Cleaning Disinfection and Sterilization................................................................................................15 4.0 STORAGE AND SHIPPING............................................................................17 4.1 Prepare for Storage..............................................................................................................................17 4.2 Shipping Preperation...........................................................................................................................17 5.0 LIMITED WARRANTY REV 0907...................................................................18 5.1 Specific Warranty Modifications..........................................................................................................18 5.2 Specific Warranty Modifications for Self-Contained Systems..............................................................18 5.3 Specific Supplemental Electronic Instrument Warranty........................................................................19 5.4 Replacement Parts Limited Warranty REV 0806..................................................................................19 6.0 TROUBLESHOOTING...................................................................................20 6.1 Basic Troubleshooting Guide..............................................................................................................20 6.2 Troubleshooting the Delivery Unit.......................................................................................................20 6.3 Troubleshooting the Closed Water System..........................................................................................20 6.4 Troubleshooting the Air Water Syringe................................................................................................20 6.5 Troubleshooting the Handpieces.........................................................................................................21 6.6 Troubleshooting the Fiber Optic System..............................................................................................21 2 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 6.7 Troubleshooting the Air Compressor....................................................................................................22 6.8 Troubleshooting the Vacuum Pump......................................................................................................22 6.9 Troubleshooting the Purge Pump.........................................................................................................22 7.0 SERVICE......................................................................................................23 7.1 Repair Service......................................................................................................................................23 7.2 Replacement Parts...............................................................................................................................23 7.3 Repairing an Air/Water and Air Only Syringe......................................................................................23 7.4 Replacing a Fiber Optic Bulb...............................................................................................................24 7.5 Servicing the Foot Control...................................................................................................................24 7.6 Opening Cover to Delivery System......................................................................................................24 7.7 Adjusting Handpiece Pressure.............................................................................................................25 7.8 Opening Back Panel............................................................................................................................25 7.9 Servicing or Replacement of Air Compressor (85-0001)....................................................................25 7.10 Replacing the Vacuum Pump...............................................................................................................27 7.11 Replacing Tubing in Purge Pump.........................................................................................................28 8.0 SCHEMATICS...............................................................................................29 8.1 Schematic, Delivery System Tubing......................................................................................................29 8.2 Schematic, Electrical 115V~ 60 Hz Voltage Selected.........................................................................30 8.3 Schematic, Electrical 230V~ 50 Hz Voltage Selected.........................................................................31 8.4 Schematic, Electrical Wiring of Delivery System (Upper Compartment)..............................................32 8.5 Schematic, Wiring Diagram 115V~ 60 Hz – Terminal Block 1 (Upper Compartment)......................33 8.6 Schematic, Wiring Diagram 230V~ 50 Hz – Terminal Block 1 (Upper Compartment).....................34 8.7 Schematic, Electrical Wiring –Compressor and Vacuum Utilities (Lower Compartment)....................35 8.8 Schematic, Pressure Switch – Air Compressor (Lower Compartment)................................................36 9.0 ILLUSTRATED PARTS LIST.............................................................................38 9.1 Delivery System....................................................................................................................................38 9.2 Delivery System Rear View...................................................................................................................40 9.3 Closed Water System, Self Contained (PN 80-0215)..........................................................................42 9.4 Air/Water Syringe (PN 20-0008)........................................................................................................44 9.5 Air Compressor, Complete Assembly (PN 85-0001)...........................................................................46 9.6 Air Compressor, Main Component (PN 40-0019)..............................................................................48 9.7 Vacuum Pump, Complete Assembly (PN 85-0002)............................................................................50 9.8 Vacuum Pump, Main Component (PN 40-0020................................................................................52 9.9 Air Tank, Dual Bracketed Complete Assembly (PN 80-0192).............................................................54 9.10 Amalgam Separator (PN 80-0188).....................................................................................................56 9.11 Purge Pump (PN 80-0214)..................................................................................................................57 9.12 Foot Control, Wet/Dry (PN 80-0112)..................................................................................................58 9.13 Service Parts Kit (PN 95-0107)............................................................................................................60 9.14 Cross Reference Parts List....................................................................................................................62 ASI- The leader in Advanced Systems Integration www.asimedical.net 3
Triton™ 2021 Manual 1.0 PRODUCT DESCRIPTION, INSTALLATION, AND SAFETY PRECAUTIONS 1.1 Safety Precautions and Warnings ! In addition to observing the normal precautions associated with standard dental practices and procedures, the following precautions should be strictly noted and observed during the set-up, operation and maintenance of this system. Warning- Compressed Air The compressed air system that operates this unit is under pressure. Compressed air can propel dust or loose particles and can cause bodily injury or damage. Always turn the system off and bleed off air pressure before attaching or removing air lines or accessories or servicing this unit. All air lines should be periodically inspected and replaced if worn or damaged. If an outside compressed air supply is used to power this unit, the air supply must be regulated to 80 psi or below. Excessive air pressure could cause certain components to rupture. Warning- Electrical Voltage This system is powered by high voltage electricity. Like any other electrically powered device, if it is not used properly, it can cause electrical shock. Always plug the power cord into an electrical outlet with adequate fuse protection and proper grounding. In the event of a short circuit, grounding reduces the risk of shock by providing an escape wire for the electric current. Improper grounding of the unit can result in a risk of electric shock. Always unplug the unit before doing any service or repair to the unit. Warning – Presence of Heavy Metals/Amalgam This cart may be equipped with optional suction instruments. As part of dental procedures, particles of amalgam may be suctioned into the dental suction handpieces and collected within the system and trap filter. Electromagnetic Compatibility (EMC) Changes or modifications to this product not expressly approved by the manufacturer may result in increased emissions or decreased immunity performance of the product and could cause EMC issues with this or other equipment. This product is designed and tested to comply with applicable regulation regarding EMC and shall be installed and put into service according to the EMC information stated below: WARNING Use of portable phones or other portable or mobile radio frequency (RF) emitting equipment near the product may cause unexpected or adverse operation. WARNING The use of accessories, transducers and cables other than those supplied may result in increased emissions or decreased immunity performance of the product. The product shall not be used adjacent to, or stacked with, other equipment. If adjacent or stacked use is necessary, the user shall be responsible to test to verify normal operation in the configuration in which it is being used. CAUTION – Federal law restricts this device to sale by or on the order of a dentist or physician. CAUTION – Check the correct operating voltage on the rating plate and ensure that the product is correctly configured for the voltage before plugging in and energizing. CAUTION – Workplace safety protocols to safeguard against cross contamination of infectious disease should always observed. When emptying the contents of the suction waste container, safe precautions and practices including the wearing of face mask, eye protection and gloves are to be followed. CAUTION – The Product should only be operated by qualified personnel only. The operator bears responsibility for the correct settings and proper use of the system. ASI Medical, Inc. (ASI) cannot be held liable for any malfunction of this product, or performance failure and/or its designed or desired utility, nor can ASI be held liable for injuries to persons or animals, in any case when the device is misused or not operated, applied or maintained in strict accordance with user/owner instructions set out in the operation manual. In the event of any doubt or question, the user is to contact ASI for clarification or assistance. 4 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual CAUTION – Responsibility for the use of accessories, parts or assemblies from other manufacturers rest solely with the user. 1.2 Product Description, Function and Intended Use The Model 2025M Triton Dental System product is a self contained dental treatment unit requiring only a connection to a proper electrical power supply for operation. It contains an internal regulated air compressor system with air tank and a vacuum pump system with holding tank and purge pump and an internal two liter clean water supply that together provide operation of dental air driven tools and evacuation handpieces used in oral evacuation. The product includes three air driven handpiece connections, air/water syringe, saliva ejector and high volume evacuator. The system does not include dental high or low speed handpieces (drills) which are to be separately supplied by the operator. The product is constructed of aluminum chassis with powder coat paint finish, high grade dual wheel type casters and composite work surface top. The product is hard wired with the appropriate type mains plug provided for the electrical specification Model as listed. The system functions to operate dental handpieces in capability expected by standard dental treatment unit. The intended use of the system is only intended to support normal dental treatment and hygiene procedures and operation of dental instruments by or under the supervision of a licensed dentist or a hygienist if permitted by applicable law. Figure 1.2-A Figure 1.2-B ASI- The leader in Advanced Systems Integration www.asimedical.net 5
Triton™ 2021 Manual Theory of Operation The Advanced Delivery System is a pneumatically controlled system that uses standard compressed air for operation of dental tools and accessories and for pressurizing a closed water supply. The system uses air pressure from a foot control to operate air driven tools and also to provide a signal to turn electric instruments on and off. This pneumatic control capability provides flexibility in that additional instruments can be included on the system for operation from the same foot control as described below: Handpiece Control and Operation The system utilizes common industry type technology for selection and activation of air driven drills and instruments via a five (5) position control block. The block contains individual gasket diaphragms that are held in the closed position by compressed air supplied by the handpiece holders. When a dental handpiece is removed from its holder, the compressed air is relieved off the gasket diaphragms for that particular instrument thereby allowing compressed air and water to flow to the handpiece when the foot control is depressed. The flow rate of this compressed air is controlled by individual stems on the top of the block and the flow of water by individual needle valves with knobs located on the front and side of the unit. Electric instruments such as the ultrasonic handpiece and electric motor are controlled via the same control block. However the compressed air that flows from the block is routed to an air/electric switch that uses an air driven piston to close contacts when activated to thereby send an electric signal for the ultrasonic and electric motor to operate. When the foot control is released, these instruments will then turn off. The System uses an air driven poppet style foot control valve that when depressed will send compressed air to the control block to operate whichever handpiece is removed from its holder. The foot control also features a toggle valve for selecting water to spray from the handpieces. When the toggle is activated and the foot control is depressed, it will allow an air signal to travel through the foot control tubing to open a water relay valve allowing water to flow to the selected handpiece. When the foot control is released it will exhaust off the air to the water relay valve and allow it to shut. Closed Water System The Closed water system uses two one liter plastic bottles designed for holding pressure. The bottles can be filled with clean tap or distilled water for the source of water supply to the dental drills and air/water syringe. The system works by supplying compressed air regulated to 35 psi which pressurizes the water within the bottle and forces it up through a plastic pick up tubing in the bottle. Quick Start Up List The operator is expected to fully read and understand all aspects of the operation manual for operation of this dental system. The following is a brief condensed highlight of steps to use the system. Verify Mechanical Integrity and Safe Use – After unpacking the unit, look for any damage that could affect safe and proper operation. Ensure there are no missing parts or accessories. Carefully inspect components for tightness and the absence of cracks, excessive wear or frayed electrical cords. If there is any adverse damage or the lack of mechanical integrity that would prevent the safe use or operation of the system, it should not be used until repair or replacements correcting the defects are made. Verify Handpiece Placements – Ensure all handpieces are placed into their correct holders and that the corresponding tubing is correctly situated. This system uses auto holders that activate the instrument once it is removed. If any instruments are incorrectly placed into holders, the selected instrument by the operator will fail to work. Quick Check – Verify all tubings hanging straight down are not crossed and are placed in sequential order from left to right on the holder bar. This will ensure they are placed correctly. Verify Holder Switches are Active – The auto handpiece holders feature a lock out switch levers which can be used to disable function of that instrument if desired by the operator. Ensure all these levers are pointing straight down towards the 6 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual floor to ensure all holders are set to active. Otherwise an instrument may fail to operate when removed from the holder. Verify Water System – Check and or fill water bottles appropriately and ensure the air pressure switch is turned on and that air pressure in the gauge reads approximately 30-35 psi. NOTE: For systems that have been stored and are being used first time, disinfect the water system by running an approved disinfectant throughout the water lines before patient use. Follow your approved protocol for disinfecting dental water lines. Verify Handpiece Operation – Handpiece instruments can be picked up and operated briefly by pressing the foot control. Verify fiber optic illumination systems light and operation of other instruments. Water can also be sprayed from instruments to ensure it is working correctly. 1.5 Unpacking and Setup Carefully remove all packaging material from around and underneath the unit and remove the accessory box, which may contain additional items required for installation. Inspect the unit for any obvious signs of shipping damage. If any damage is discovered, immediately contact our Customer Service Department at (800) 566-9953. Roll the unit to its location on a level surface. Place the handpiece tubings, optional instruments, the air/water syringe and the high and low volume evacuation valves into their respective holders. Position the foot control and tubing on the floor toward the front of the unit. Locate the clean water system inside the door on the side of the system. Fill the bottles with clean water or other approved solutions. Please refer to 2.3 Clean Closed Water System for more information. 1.3 Electrical Installation Once the correct voltage selection has been verified and configured if necessary, unwind the power cord from the back of the unit and plug into an appropriate electrical outlet. Turn the unit on by switching ON the Main Power switch, located at the rear of the system. To turn on the air, switch ON the Air switch, next to the Main Power switch. The air compressor will turn on and begin pressurizing the system. The air compressor will automatically shut off after a few minutes when the air tanks have reached full pressure. To turn on the suction, switch ON the Suction/Vacuum switch, next to the Main Power switch. The vacuum pump will run as long as this switch is on. 1.4 Installation of the Optional Purge Hose Quick Connect Kit Model 90-2712 General Information: Dishwasher installation kits are readily available from your local plumbing supply store. These kits normally contain the items that allow you to connect the purge hose to a sink drain using a dishwasher Branch Tailpiece. Depending on your application, it may be necessary to substitute components to match the plumbing fixtures used with your sink. If you need additional information, please consult with a plumber to assist you with the installation. These dishwasher installation kits usually contain the following items: Dishwasher Branch Tee Flanged Washer 90-2712 Rubber Connection Boot Hose Clamp The items contained in the Purge Hose Quick Connect Kit are: Plastic Discharge Hose 3/8” ID Bulkhead Connector Fitting Installation Step 1: Connecting the Dishwasher Branch Tailpiece 1. Follow the instructions in the plumbing supply kit for installing a dishwasher branch tee. Figure 1.4 ASI- The leader in Advanced Systems Integration www.asimedical.net 7
Triton™ 2021 Manual Step 2: Attaching the Rubber Connection Boot 1. Place the rubber connection boot over the tailpiece branch and tighten clamp (see figure 1.7 – A). 2. Insert the discharge hose into the other end of boot and tighten clamp. Step 3: Installing the Bulkhead Connector Fitting 1. D etermine a location on the front or side of the sink cabinet for placement of the bulkhead connector. 2. Drill a 3/4” hole into the cabinet using a drill bit or hole saw. 3. Remove the nut from the bulkhead connector and place the bulkhead connector through the 3/4” hole in the cabinet (the hose barb end of the connector should be placed to the inside of the cabinet) and tighten the nutsecurely. NOTE: If the wall of the cabinet is too thick, it may be necessary to file away excess material from the inside cabinet surface in order to attach the nut to the bulkhead threads. 4. P lace the hose clamp over the discharge hose, and push the hose fully onto the barb of the bulkhead connector. Tighten the hose clamp firmly. Step 4: Checking the Installation 1. Unwind the purge hose from the back of the self contained system and place the male connector into the bulkhead fitting. 2. Using the oral evacuation system, pump clean water into the waste container and pump out using the purge pump switch. 3. Check for leaks. If some leaks appear, additional tightening of nut(s) may be needed. If leaks continue, turn off the system and disconnect. Loosen plumbing attachments, check alignment of washer(s) and tighten again. 1.5 Optional Installation to Utility Center Systems Self contained systems may also have an option to be connected to a central air supply and optional vacuum. Connection of umbilical lines from the cart to an appropriate junction box are the responsibility of the user and should only be performed by knowledgeable individuals. Figure 1.5-A Figure 1.5-B 8 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 1.6 Dimensional Specifications, Capacities and Technical Data, Triton™ 2025M Technical Specifications Construction: High grade aluminum sheet metal Finish: Baked-on powder coat Dimensions: 19.5” (50 cm) W 225” (70 cm) D 35.5” (90 cm) H Weight: 150 lb. (75 kg) Water System Reservoir Capacity: 2–1.0 liter bottles Operating Pressure: 35 psi (2.5 bar) Aseptic, non-retracting water system. Electrical System Mains Power 115 Volts / 60 Hz or 220 Volts / 50 Hz Type: B Compressor System Type: Oil-less piston Duty cycle: Intermittent Duty Working Pressure: 80–100 psi (5.5 – 6.9 bar) Flow rate: 2.5 cfm Sound level: 46 dB measure at 3’ (1m) Air reservoir: 4 liters Air drying: After-cooler with pneumatic filter Vacuum System Type: Oil-less piston Duty cycle: Intermittent Duty Vacuum: Adjustable 5” - 20” Hg Vacuum flow: 5.5 cfm free flow Waste receptacle: 4 liters Waste purge tubing: 12’ (4m) L Sound level: 43 dB measure at 3’ (1m) Automatic overflow shutoff Aseptic, filtered exhaust Solids trap ASI- The leader in Advanced Systems Integration www.asimedical.net 9
Triton™ 2021 Manual 1.7 Operating Environment and Classification of Equipment Classification of Equipment (EN-60601-1) Type/Mode Classification Types of shock protection Class II Equipment: Chair, wall, and cart delivery systems Degree of shock protection TYPE B APPLIED PART: Delivery systems only Degree of protection against water ORDINARY EQUIPMENT ingress Mode of operation Intermittent Flammable Gasses: Not suitable for use in the presense of a flammable anesthetic mixture with air, oxygen, or nitrous oxide, where such gasses may accumulate in concentration (closed spaces). Environmential Specifications Temperature/Humidity Specification Storage/Transportation Temperature: -40˚C to 70˚C (-40˚F to 158˚F) - Relative humidity 80% Operating Temperature: 10˚C to 40˚C (40˚F to 104˚F) - Relative humidity 80% Indoor Use: Altitude up to 2,000M (6,563 ft.), installation category II, polution degree 2. (UL 61010A-1 and CAN/CSA C22.2, No. 1010.1-92 only) Identification of Symbols Symbol Description Recognized by Underwriters Labratories Inc. with respect to electric shock, fire, and mechanical hazards only in accordance with UL 61010-1 (2601-1) and under mutual recognition agreement with CAN/CSA C22.2, No.601-1. Protective earth (ground). Functional earth (ground). Attention, consult accompanying documents. No user servicable parts. Attention, line voltage. Only ! licensed electrician should remove cover. Type B applied part. Class II Equipment. Caution: Metal surfaces can be hot during and following the dry cycle. 10 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 2.0 COMPONENT OPERATING INSTRUCTIONS 2.1 Clean Closed Water System The Dual Closed Clean Water System (see figure 2.1-A) features easy-to-fill, pressurized water bottles that enable you to provide clean water and control the quality of water to your handpieces and air/water syringe. The water bottle is made of non-porous plastic. It is virtually unbreakable, and it does not impart an after-taste to the water. 2.1.1 How It Works Air, regulated to approximately 35 psi, is supplied to the water bottles through tubing attached to the bottle caps. The air pressure in the bottle forces clean water from the water bottle into the water pick-up tube and out to the handpiece control blocks, syringe, and auxiliary quick connects. The water system supplying water to the oral cavity is now a “closed system,” allowing you to control water quality and water system asepsis. 2.1.2 Filling the Bottles Locate the Dual Closed Clean Water System (may be mounted inside the unit or on the exterior). Locate the toggle switch for supplying air pressure to the bottles. Figure 2.1-A Flip the switch to the OFF position to turn off the air supply to the bottles. Unscrew the bottles and clean as appropriate. Fill the bottles with clean or distilled water to a level just below the screw threaded portion. Re-attach the bottles and hand tighten only. If using distilled water, it is recommended that some type of antimicrobial agent, approved safe for dental procedures, be added to prevent potential bacterial growth in the system. 2.1.3 Operating the Dual Closed Clean Water System The closed clean water system features a selector valve that allows the operator to choose solution from bottle 1 or bottle 2. Turn the air pressure toggle switch to the ON position and ensure that the selector switch is flipped to the bottle containing the desired solution. The system will now provide solution to the delivery unit and corresponding handpieces. 2.1.4 Disinfecting the Water System Refer to Cleaning and Disinfection Section of the Manual for disinfection of the clean water system 2.1.5 Purging Water From the System Running compressed air through the water lines is an easy and effective way to remove water from the lines and prevent stagnant water from residing in the lines during temporary or long term storage of the system. To purge the water, remove the bottles and completely empty them of their liquid contents. Then replace the bottles and turn on the air pressure supply to the bottles. Run the handpiece connections and air water syringe until there is no more water particles exiting them. The lines will now be sufficiently dry for storage. 2.2 Air/Water Syringe Check the flow of air, water and spray from the syringe. Press the right button for water stream. Press the left button for air. Press both simultaneously for spray. To adjust the flow of air, turn the syringe air adjustment knob clockwise to increase, counter-clockwise to decrease. To adjust the flow of water, turn the syringe water adjustment knob until the desired level of flow is achieved (see Figure 2.2-A). 2.2.1 Tip Removal and Replacement To remove the syringe tip, press down on the outside collar. When you feel a Figure 2.2-A soft click, the tip may be pulled straight out. Hold the collar down and insert the new tip. Be sure to press it all the way in, then release the collar. Test the installation by giving a firm pull on the tip to assure that it is inserted all the way, and that the locking mechanism is engaged. ASI- The leader in Advanced Systems Integration www.asimedical.net 11
Triton™ 2021 Manual 2.3 Handpieces Refer to the handpiece manufacturer’s instructions for the proper connection, use and maintenance of the handpiece prior to attaching them to this system. Connect the handpieces to the appropriate tubing connector. The handpieces are automatically activated whenever they are removed from their holder. (Ensure that only one handpiece is removed from the holder at a time to prevent multiple handpiece activation. If so equipped, engage the handpiece lockout feature for additional safety.) Handpiece holders can slide from side to side on the bar, they can ratchet around the bar, and they can be rotated. For instrument handpieces, a manual lockout lever shuts the holder off so the instrument can be removed without having it activated by the rheostat. To engage the lockout, lift the lever to a horizontal position. To return the holder to normal operation, point the lever back down to the floor. 2.3.2 Coolant Operation – Adjusting Coolant Spray To activate the coolant water for a handpiece flip the toggle switch either located on the front of the system or on the foot control. To deactivate the coolant water, flip the toggle switch to the OFF position. To adjust coolant spray, locate the adjustment knob on the unit on the side or front. Turn the toggle switch for coolant spray to ON, then turn the adjustment knob (clockwise to decrease, or counter-clockwise to increase) until the desired level of spray is achieved (see Figure 2.3 - A). Note: For multiple instruments that provide coolant, individual adjustments are provided and are located in order from left to right. Figure 2.3-A 2.4 Fiber Optics To determine the style of fiber optics you will need for your handpiece, look at the back of your handpiece or the swivel coupler and compare the connections to the following drawings. For bulb replacement please refer to Service section of this manual. 2.4.1 Five Hole Fiber Optic Systems Popular in the U.S., these systems are an adaptation of the four hole handpiece connection, simply by adding a fifth hole for the light to enter the back of the handpiece. The light travels from the bulb up through the swivel coupler and through the handpiece via fiber optic glass rods. 2.4.2 Six Pin Fiber Optic Systems Standard in Europe, these systems are also used in the U.S. due to the influence of European brand handpieces sold in the U.S. These systems are similar to five hole systems; however, instead of having the small bulb in the connector at the end of the tubing, the bulb is contained in the swivel coupler from the handpiece. The connector at the end of the handpiece tubing has two electrical sockets that connect to the two small wires. The swivel coupler has two electrical pins that drop into these sockets when it is attached. Unless specifically requested, units purchased with optional Universal Fiber Optics are set to a five hole configuration at the factory. To modify a five hole handpiece tubing to work with a six pin fiber optic handpiece, remove the fiber optic bulb from the handpiece tubing and insert the ISO adapter provided in your Accessory Kit. First, remove bulb. Replace bulb with adapter. 12 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 2.4.3 Fiber Optics Operation In order for fiber optics to work, the fiber optic handpiece must be attached to the handpiece tubing. Once the handpiece has been removed from its holder, press the foot control to activate the fiber optics. The specific handpiece air pressure may need to be increased to create the back pressure, depending on the type of fiber optic handpiece you are using. Please refer to Adjusting Handpiece Pressure for more information. 2.5 Oral Evacuation System How It Works To use an evacuation handpiece, remove the valve from the holder and insert the desired tip into the valve. The saliva ejector valve accommodates standard saliva ejector tips and the HVE valve accommodates standard 7/8” tips. To ensure maximum suction flow, periodically check and replace the solids trap screen located on the front of the system. Remove the cover to the solids trap, lift out the old screen, insert the new screen and replace the cover to the solids trap. 2.6 Self-Contained Vacuum Pump The vacuum pump is activated when the Suction/Vacuum On/Off switch, located on the rear of the unit, is in the ON position. To use, open the lever on the evacuation handpiece. To maximize vacuum strength of the evacuation handpiece, close the lever valve of the other evacuation handpiece whenever it is not in use. Note: The strength of the vacuum pull to the oral evacuation system is regulated by the vacuum relief valve. The relief valve on the system is pre-set to approximatley 12” Hg. Please refer to the 3.2 Purging the Waste Canister and Cleaning the Evacuation System for more information. 2.7 Suction Canister with Amalgam Separator The system includes a suction canister for holding liquid contents obtained from evacuation by the suction handpieces. The contents must be emptied daily. The suction canister has an overflow switch to help prevent accidental overfilling of the canister. However it is important to empty the liquid before it reaches capacity to prevent potential liquid being pulled into the vacuum pump. Follow the instructions under maintenance for purging and cleaning the suction system. The bottom of the suction canister has a sediment bowl which is designed to provide an internal amalgam separator. The system uses the settling method for heavy particles including fine particles of dental filling amalgam to be captured in the sediment bowl. The sediment bowl should be checked every three months. See Maintenance instructions for checking and replacing the Amalgam Separator bowl. ASI- The leader in Advanced Systems Integration www.asimedical.net 13
Triton™ 2021 Manual 3.0 MAINTENANCE 3.1 Equipment Care and Inspection The equipment should be thoroughly cleaned and disinfected after use each day to maintain optimal performance. The following visual checks and inspections should be performed before operating the unit: Look for mechanical damage that could affect safe operation. Ensure there are no missing parts or accessories. Inspect components for tightness, cracks, wear or frayed electrical cords. Should mechanical or other damage be evident that would affect the safe use or operation of the system, it should not be used until repair or replacements correcting the defects are made. 3.2 Purging the Waste Canister and Cleaning the Evacuation System The canister should be purged and the oral evacuation system cleaned whenever the waste collection canister is full, or at the end of the day’s treatment procedures. IMPORTANT: The vacuum receptacle has an overflow shut-off device to prevent the canister from being over-filled with liquid flowing into the vacuum pump. It is important to regularly empty this container to avoid inadvertently filling the canister to capacity during a treatment procedure. To purge the contents from the canister, position or move the unit near a sink or other acceptable sewer drain. Unwind the purge tubing, located on the back of the unit Place the end of the tubing into a sink drain or other acceptable receptacle. Locate the waste pump toggle switch on the back of the unit, above the waste purge tubing. Flip the switch ON to purge the contents of the waste collection canister. ! IMPORTANT: The waste pump will remove the liquid under high pulsating pressure. Therefore, it is necessary to hold the hose by hand or ensure that it is firmly in place before pumping out the contents. Note: For “hands free” purging of the system, the tubing can also be connected to a receptacle to drain directly into the “P” trap of sinks Please refer to 1.5 Installation of Optional Purge Hose Quick Connect Kit for more information. After the waste contents have been emptied, fill a one quart reservoir with any properly prepared NON-FOAMING vacuum cleanser or ASI’s Evacuation System Cleaner (P/N 95-0101). Using the high volume evacuator, suction the prepared cleaner solution into the system and leave overnight, or longer, if necessary. This will allow the enzyme solution to properly clean. Purge contents before starting dental procedures. Suction one ounce of concentrated vacuum cleanser prior to the day’s dental procedures to start enzyme breakdown as fluids are drawn in to system. ! CAUTION: Due to its caustic nature, DO NOT use BLEACH as a disinfectant, as it will corrode certain internal parts. Small amounts used as an irrigating solution for dental procedures is acceptable. 14 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 3.3 Amalgam Separator Bowl Checking and Replacement To remove the sediment bowl have a qualified service personnel open the back panel of the delivery system. See Service instructions for access. The amalgam separator is located on the left above the vacuum pump. Loosen the Velcro straps under the separator (see Figure 3.3 - A). Grab the sediment bowl with both hands and remove by rotating while pulling down (see Figure 3.3 - B). Once the bowl is removed, empty the contents into an appropriate hazardous waste receptacle to send to an authorized mercury disposal service provider. Replace the bowl by sliding it into the amalgam separator until seated. Secure with the Velcro straps. Close the back panel and secure. Figure 3.3-A Figure 3.3-B 3.4 System Air Pressure An air filter/regulator (see Figure 3.4 - A) controls system air pressure and is preset to 65-75 psi. The air/filter regulator is located inside the unit, at the base of the aluminum air tanks. To access, remove the panel screws and open the back panel. Read the air gauge provided. If the system pressure is not 65-75 psi, simply lift the adjustment knob and turn clockwise to increase pressure or counter-clockwise to decrease pressure. To release excess pressure, press the Air Syringe button before reading the gauge. When the desired pressure is reached, push the adjustment knob back down to lock it in place and prevent accidental pressure change. 3.5 Cleaning, Disinfection and Sterilization 3.5.1 Wilsonart™ Care and Maintenance Figure 3.4-A Follow the guidelines listed below to keep your Wilsonart™ composite solid surface worktop looking as good as new. ASI- The leader in Advanced Systems Integration www.asimedical.net 15
Triton™ 2021 Manual Routine Care Most dirt and stains Use soapy water or ammonia-based cleaner. Water marks Wipe with damp cloth; towel dry. Use an abrasive cleanser and a green Difficult stains Scotch-Brite™ pad. Occasionally wipe surfaces with diluted Disinfecting household bleach (1 part water/1 part bleach). Maintenance Rub with Scotch-Brite™ pad alone. Sand with 180- or 220-grit fine sandpaper until cut is gone. Restore finish with an Removing Cuts and Scratches abrasive cleanser and a green Scotch-Brite™ pad. 3.5.2 Disinfecting the Dual Closed Clean Water System and Handpiece Tubing There are many disinfectant protocols that are acceptable for use with the ASI closed clean water system, such as popular brands of tablets and antimicrobial solutions. Please follow those manufacturers guidelines. CAUTION: Due to the caustic nature of bleach, DO NOT USE in this system. It can corrode certain internal parts and will void warranty coverage of these components. If desired, you may fill the bottle(s) with a solution of 10 parts water and 1 part mouthwash, such as SCOPE, or another type of disinfectant. For more information on this protocol, please see abstract entitled “A Chemical Treatment Regimen to Reduce Bacterial Contamination in Dental Water Lines” in the May 1997 issue of JADA. If using another type of disinfectant, follow the instructions provided with your disinfectant for effective control of the growth of biofilms in the water lines.c 3.53 Syringe Tips Tips may be sterilized by steam autoclave, ethylene oxide gas, or chemical vapor process. Maximum sterilization temperature is 280º Fahrenheit (138º Celsius). Be sure to thoroughly rinse all cleaning agents from the tips before sterilization. This is particularly important when using chemical vapor because cleaning agents may react with sterilization chemicals and form crystals that can clog the tips. 16 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 4.0 STORAGE AND SHIPPING 4.1 Prepare for Storage To prepare for either storing or shipping, follow the instructions below: 1. Empty the water containers and purge handpiece coolant lines and the water syringe. See Operation Instructions. 2. Purge the waste container and flush clean. 3. Remove and dispose of solids trap filter and the HVE and saliva ejector tips. 4. Unplug unit from power and carefully wind the purge hose and power cord around the brackets on the rear of the cart. ASI- The leader in Advanced Systems Integration www.asimedical.net 17
Triton™ 2021 Manual 5.0 LIMITED WARRANTY REV 0907 ASI Medical, Inc. (ASI) warrants this product against defects in material and/or workmanship for one year for parts, 90 days for labor, from the time of delivery. During this coverage period, ASI’s sole obligation will be to repair, adjust or replace defective parts only. ASI is not responsible for any time lost, inconvenience caused, or for any other incidental or consequential damages. The warranty shall be voided by alteration (except by ASI), tampering, improper installation or maintenance, accidental damage, or misuse of the product. This warranty is made in lieu of all other warranties, expressed or implied, including any implied warranty of merchantability of fitness for particular purpose. No employee, agent, franchise, dealer or other person is authorized to give any warranties of any nature on behalf of ASI, except as provided herein. ASI shall have no liability or responsibility to the customer, any other person, or entity with respect to any liability, loss, or damage caused directly or indirectly by the product. Notwithstanding the above limitations and warranties, ASI’s liability hereunder for damages incurred by the customer or other shall not exceed the amount paid by the customer for the particular product involved. ASI shall not be responsible for any warranty work done without first obtaining consent from ASI. 5.1 Specific Warranty Modifications The following items and/or occurrences are not covered under the warranty: Accidental Damage & Theft, including but not limited to the following: •D amage from accident or misuse including cuts, tears and crushes to tubing, cracks in suction solids trap filters, housings, broken casters, etc. • Damage from use including scratches, dings, dents and deterioration to paint and overlays • Theft or vandalism Damage from Neglect or Improper Maintenance, including but not limited to the following: • O-ring lubrication to valves in the air or water syringes and foot controls • Flushing of handpiece or micro irrigation lines • Removal of condensation from air lines •O bstructions in water lines and handpiece tubing caused by foreign particles or chemical agents dispensed through the lines • Obstructions in suction lines caused by foreign particles or improper maintenance of trap filters Disposable Type Items including but not limited to the following: • Light bulbs, all filters, and certain types of tubing 5.2 Specific Warranty Modifications for Self-Contained Systems The following items and/or occurrences are not covered under the warranty for Self-Contained Systems with Internal Air Compressor And/Or Suction Systems: Damage, Clogs or Malfunctions to Canister and Purging System – Due to the inability to control items and solutions that are pulled into the suction system and their proportion levels, including but not limited to adhesives, cements, impression materials, caustic Endodontic irrigants; and the unpredictable maintenance regime that may be followed to mitigate clogging or malfunction, the suction canister, its components, the purge pump of the suction system, and the tubing is excluded from warranty coverage. Damage to Vacuum Pump from Liquid Contamination – The waste canister has an overflow float switch that will cut power to the vacuum pump in the event the canister begins to fill completely. This will prevent liquid and other contaminants from being pulled into the internal pistons of the vacuum pump. However, improper maintenance can result in a malfunction of the overflow float switch or constant overfilling of the canister can result in liquid contamination of the vacuum pump. This type of damage is specifically excluded from warranty coverage. Damage to Vacuum Pump and Air Compressor from Chemical Vapor Contamination – If certain caustic chemicals used in dental procedures (specifically bleach used in Endodontic procedures) is repeatedly used in concentrated forms without rinsing 18 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual with water, this can cause highly concentrated gases to be pulled into the vacuum pump and air compressor system, causing corrosion to the internal working components. Corrosion damage to the vacuum pump or the air compressor system from chemical gases is specifically excluded from warranty coverage. 5.3 Specific Supplemental Electronic Instrument Warranty As a convenience to our customers, ASI offers to install new or used brands of instruments, not manufactured by ASI, into our systems. This benefit enables customers to configure their systems with various instruments and to realize the cost savings of incorporating already owned instruments. ASI’s standard one year warranty is further modified for these installed instruments, as follows: ASI’s supplemental warranty does not extend the original term of the manufacturer’s warranty, include items not covered under the manufacturer’s warranty, or warranty problems caused by, or resulting from, misuse or accidental breakage. Any installed instruments requiring repair will need to be removed and sent back to the respective manufacturer for inspection and repair. It will be the responsibility of the customer for any labor costs incurred in the removal, replacement, shipping, or packaging of these instruments. ASI will not be responsible for these costs or the ability of the manufacturer to complete any necessary repairs in a timely manner. ASI Medical, Inc. will provide a supplemental warranty for a period not to exceed one year from the date of purchase of new components from other manufacturers that are installed into ASI delivery systems. This supplemental warranty is only valid in the event that the component manufacturer declines to honor its warranty due to the component’s removal from its original housing. In the event the manufacturer declines to honor its warranty for an item that otherwise would have been covered, ASI will reimburse the customer for the amount of the repairs billed by the instrument manufacturer, not to exceed the selling price of the instrument. 5.4 Replacement Parts Limited Warranty REV 0806 Replacement parts (either purchased or replaced at no charge warranty) do not affect or extend in any way the original warranty term provided. New replacement parts are provided with a ninety day warranty term from the time of shipment, and does not include any other costs such as labor for installation, removal or shipping. These separate costs are the responsibility of the customer. All other terms, modifications and exclusions provided in the system warranty apply to replacement parts. ASI- The leader in Advanced Systems Integration www.asimedical.net 19
Triton™ 2021 Manual 6.0 TROUBLESHOOTING 6.1 Basic Troubleshooting Guide The following information is not intended to isolate every problem that could arise with the dental system. It is, however, designed to help you quickly identify problems that can be repaired without any special equipment or training. 6.2 Troubleshooting the Delivery Unit If the system is maintained and given proper care, it will provide reliable service. If something does go wrong, the information contained herein explains what can be done prior to physically removing the unit for extensive repair. If this information does not identify and correct the problem, more detailed information is available in sections covering the individual components. Problem Possible Cause Correction Audible air leak from inside the control Loose fitting or tubing Open the cover. To find the leak, apply panel a soapy solution to connections. When leak is found, tighten or replace leaking components. Water leakage from within control Loose fitting or hole in tubing Apply water pressure, complete a visual panel check for leak. Tighten or replace leaking components. Air bubbles in the coolant water and Low water level in clean water container Refill container. syringe water flow Leak in water relay valve Replace valve. Reduced or no flow of air or water Loose fitting Check all water fastener connections and tighten if necessary. Blocked or pinched tubing Make sure tubing is not pinched. If tubes are not pinched, inspect for blockage. 6.3 Troubleshooting the Closed Water System Problem Possible Cause Correction No Air Pressure Switch not on. Turn Air Pressure to On. Faulty air regulator Replace in-line regulator Water not coming out. Bottle empty Verify selector is turned to bottle 1 or 2 and that water is in that container. 6.4 Troubleshooting the Air Water Syringe Problem Possible Cause Correction Valve cartridge leaks water. Worn O-rings Replace O-rings or valve assembly. Valve cartridge button sticks. Debris build up Clean module cavity and valve cartridge assembly. Worn O-rings Replace O-rings. Worn valve spring Replace spring. Nozzle tube connection leaks water/air. Loose connection Check connections. Worn O-rings Replace O-rings. Clogged nozzle tube Debris from delivery system tubing or Run cleaning wire through nozzle tube sterilization deposits and ultrasonically clean. Spray mist occurs when depressing air Worn nozzle assembly O-rings Replace O-rings. valve immediately following water valve depression. 20 ASI- The leader in Advanced Systems Integration www.asimedical.net
Triton™ 2021 Manual 6.5 Troubleshooting the Handpieces Problem Possible Cause Correction Low pressure to handpieces Low pressure from compressor or Check air pressure gauge. Ensure 75 regulator in junction box psi prior to adjusting handpiece block. Air adjustment screws on control block Turn adjustment screws (recessed in are closed or adjusted too low. console) counter-clockwise to increase pressure. Two or more handpieces run when only Handpiece may not be seated properly Check that placement in holder one should. in holder. properly shuts off micro switch at the base of the holder. Water leaks from handpiece when Defective water relay Inspect water relay for proper function. switch is on, but handpiece is not in Replace if necessary. use. Handpiece may not be seated properly Check that placement in holder in holder. properly shuts off micro switch at the base of the holder. None of the handpieces work (no air or Pinched or crimped foot control tubing Check tubing and remedy or replace water). tubing. Water to 3-way syringe but there is not Needle valve off or pinched water line Ensure needle flow control valve is water to the handpieces. opened. Water switch on foot control or control Turn on water switch. panel turned off Defective water relay Replace water relay. Water toggle switch defective Replace switch. Tubing for air signal from toggle switch Correct tubing. is kinked. Air escaping from handpiece when not Hole in gasket puck in control block. Replace gasket. in use. Water leaks from handpiece when not Hole in gasket puck in control block. Replace gasket. in use. 6.6 Troubleshooting the Fiber Optic System Problem Possible Cause Correction No Light Bulb loose Secure bulb in socket. Bulb burnt out Replace bulb. Power supply cord loose Push firmly into receptacle. Faulty air signal to lamp control Check air signal tubing connection on lamp control box. Loose wiring Check wires connecting to the lamp control box, transformer and handpiece tubing. If a loose wire is found, refer to wiring schematic and manufacturer’s repair diagrams. 6.7 Troubleshooting the Air Compressor Problem Possible Cause Correction Air leaks Hose fitting loose Tighten fitting. ASI- The leader in Advanced Systems Integration www.asimedical.net 21
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