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Page 1 of 7 Reprocessed byInstructions for useReprocessed ViewFlex Xtra ICE CatheterReprocessed device for single useCaution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.▪STERILE▪Exposed to Ethylene Oxide (EO) gasExplanation of symbolsSymbolRules/StandardReferenceISO 7000RegistrationNumberSymbol Title DescriptionRx Only 21CFR801 N/A Prescription only Indicates Federal (USA) law restricting device to saleby or on order of a physician.ISO 15223-1Clause 5.1.1 3082 Manufacturer Indicates the medical device manufacturer.ISO 15223-1Clause 5.1.3 2497 Date of manufactureIndicates the date when the medical device wasmanufactured.ISO 15223-1Clause 5.2.3 2501Sterilized usingethylene oxideIndicates a medical device that has been sterilizedusing ethylene oxide.ISO 15223-1Clause 5.1.4 2607 Use-by dateIndicates the date after which the medical device is notto be used.ISO 15223-1Clause 5.1.5 2492 Batch codeIndicates the manufacturer’s batch code so that thebatch or lot can be identified.ISO 15223-1Clause 5.1.6 2493 Catalogue numberIndicates the manufacturer’s catalogue number so thatthe medical device can be identified.ISO 15223-1Clause 5.1.7 2498 Serial numberIndicates the manufacturer’s serial number so that aspecific medical device can be identified.ISO 15223-1Clause 5.4.3 1641Consult instructionsfor useIndicates the need for the user to consult theinstructions for use.ISO 15223-1Clause 5.4.2 1051 Do not re-useIndicates a medical device that is intended for one use,or for use on a single patient during a single procedure.ISO 15223-1Clause 5.2.6 2608 Do not resterilize Indicates a medical device that is not to be resterilized.ISO 15223-1Clause 5.2.8 2606Do not use ifpackage is damagedIndicates a medical device that should not be used ifthe package has been damaged or opened.ISO 15223-1Clause 5.3.2 0624Keep away fromsunlightIndicates a medical device that needs protection fromlight sources.ISO 15223-1Clause 5.3.3 0615Protect from heatand radioactivesourcesIndicates a medical device that needs to be protectionfrom heat and radioactive sourcesISO 15223-1Clause 5.3.4 0626 Keep dryIndicates a medical device that needs to be protectedfrom moisture.Stryker’s Sustainability Solutions ©20231810 W Drake Dr.Tempe AZ, 85283888 888 3433Reprocessed ViewFlex Xtra ICE Catheter DescriptionThe Reprocessed ViewFlex Xtra ICE Catheter is a temporary intracardiac ultrasound catheter intended for use in patients to accurately visualize cardiac structures, blood flow and other devices within the heart when connected to compatible intracardiac ultrasound console via the compatible ViewFlex™ Catheter Interface Module. Examples of the types of devices that can be visualized include, and are not limited to, intracardiac catheters, septal occluders, delivery wires, delivery sheaths, sizing balloons and transseptal needles. The use of these images is limited to visualization with no direct or indirect diagnostic use.The Reprocessed ViewFlex Xtra ICE Catheter has a useable length of 90 cm, with a 9 French (F) shaft with an ultrasound transducer. A 10F introducer is recommended for use with this catheter for insertion into the femoral or jugular veins. The catheter tip has four-directional deflection allowing for Left-Right and Posterior-Anterior deflection, with an angle of at least 120 degrees in each direction.The Reprocessed ViewFlex Xtra ICE Catheter is compatible with the ultrasound consoles listed in the table below. See table below for specifics on each ultrasound consoles.H701375 H700296 Compatible ViewFlex Catheter Interface Module 100038191 H701374100043720Maximum Viewing Depth 18 cm 18 cm 18 cm*All consoles are not available in all countries.a CX50 is a trademark of Koninklijke Philips Electronics.N.V.Indications for useThe Reprocessed ViewFlex Xtra ICE Catheter is indicated for use in adult and adolescent pediatric patients to visualize cardiac structures, blood flow and other devices within the heart.Contraindications for useThe Reprocessed ViewFlex Xtra Ice Catheter is contraindicated:▪If there is an occurrence of conditions that create unacceptable risk during catheterization.▪If the patient that has a mechanical tricuspid valve (a prosthetic tissue valve is permissible).▪If the patient has ongoing sepsis or known hypercoagulable state where the catheter could serve as a focal point for septic or bland thrombus formation.▪If the patient has any condition that, in the opinion of the investigator, contraindicates the placement and use of the cardiac catheter or internal ultrasound.Warnings▪The Reprocessed ViewFlex Xtra ICE catheter and system should be used only by or under the direct supervision of a physician thoroughly trained in sonography and ultrasound technology, or with the assistance of asonographer or physician trained in ultrasound technology.▪The Reprocessed ViewFlex Xtra ICE catheter and system should be used only by or under the direct supervision of a physician thoroughly trained in the techniques of cardiac placement during interventional andelectrophysiology procedures.▪The Reprocessed ViewFlex Xtra ICE Catheter is to be used only with the ViewFlex Catheter Interface Module, the ViewMate and the Phillips CX50 ultrasound consoles. Any other use or inappropriate electrical connection may pose a serious risk to patient safety.▪The Reprocessed ViewFlex Xtra ICE Catheter includes a 9F shaft. The physician should consider anatomical size restrictions if considering use of the ViewFlex Xtra ICE catheter on pediatric patients.▪The Reprocessed ViewFlex Xtra ICE catheter is to be used for ultrasound imaging only.▪Do not immerse the proximal handle or cable connector in fluid. Electrical performance may be affected.▪Do not use the Reprocessed ViewFlex Xtra ICE catheter if the packaging is opened or damaged.▪Do not use the Reprocessed ViewFlex Xtra ICE catheter if it is damaged.▪Tactile feedback of reprocessed devices may vary during use.Precautions▪Do not attempt to use the Reprocessed ViewFlex Xtra ICE Catheter prior to completely reading and understanding the Directions for Use.▪The Reprocessed ViewFlex Xtra Ice catheters are supplied sterile only if packaging is not damaged or open.▪Inspect the packaging and catheter for damage or defects prior to use.▪The Reprocessed ViewFlex Xtra ICE Catheters have been sterilized using EtO. Do not attempt to sterilize the catheters by autoclave, gamma or ultraviolet radiation, or liquid sterilizing solutions.▪Do not bend, kink, stretch, or forcefully wipe the catheter. These actions may damage the catheter.▪Do not use mechanical tools or forceps to grip the catheter.▪Have antiarrhythmic drugs, an external defibrillator, and respiratory assist equipment available in case of complications during the use of this device.▪The device should only be used in patients that have received anticoagulation prior or during the procedure. Adverse reactionsAlthough temporary intracardiac catheter sonography procedures have been proven to be safe, the physician should also be aware that complications can occur with the use of any cardiac catheter.Risks that may be associated with the use of the Reprocessed ViewFlex Xtra ICE catheter are those that may be encountered with the introduction and placement of temporary cardiac catheter or pacing lead. As a result of the delivery of electrical energy during internal defibrillation additional risk may result.Adverse events related to cardiac catheterization have been documented and include, but are not limited to:▪Bleeding, hematoma or thrombus at the catheter introduction site▪Cardiac irritability▪Catheter kinking or excessive bending▪Infection/sepsis▪Intercostal or phrenic nerve stimulation▪Mechanical induction of arrhythmias or asystole▪Perforation causing cardiac tamponade▪Perforation of the chamber or vessel wall▪Pneumothorax▪Pulmonary infarction▪Thrombophlebitis▪Tricuspid valve injury▪VasospasmImportant AdviceAny alleged malfunctions, deficiencies, or deterioration in the characteristics and/or performance of this device, along with any alleged inadequacy in the labeling or Instruction for Use, which might lead or have led to a serious injury or death must be brought to the attention of Stryker Sustainability Solutions.Directions for usePreparationIt is recommended practice to have on hand a duplicate of each sterilized item when introducing a catheter. In case the aseptic technique is compromised the procedure can continue.Image Quality Interference (noise)If severe RF interference is experienced during ablation procedures, relocate and/or shield the Reprocessed ViewFlex Xtra ICE catheter electrical extension and Catheter Interface Module.Catheter Insertion and Positioning1.Follow a suitable surgery protocol. The instruction are provided as a general guide and are intended forinformation purposes only, the physician may alter the catheter insertion techniques based on standard clinical practice.2.The Reprocessed ViewFlex Xtra ICE catheter is intended for use during single patient procedure. Do notattempt to resterilize. Stryker will not accept Reprocessed ViewFlex Xtra ICE Catheters for reprocessing that have been reprocessed and sterilized by other facilities.3.The package label is detachable and may be affixed to the medical record of the patient.4.Before beginning the procedure, verify overall compatibility of all instruments and accessories.5.Connect the patient to a vital signs monitor. Track patient vital signs throughout the procedure.6.Inspect packaging before opening. The contents of the package are sterile if the package has not beencompromised.7.Do not use the Reprocessed ViewFlex Xtra ICE Catheter if the sterility has been compromised. If the packageis damaged or if it was opened and the instrument not used, return the Reprocessed ViewFlex Xtra ICECatheter and the package to Stryker.8.Prepare the insertion site using cutdown or percutaneous entry technique. Use a 10F or larger introducersheath.NOTE: It is possible to transfix the femoral artery during percutaneous entry into the femoral vein. Follow proper femoral vein puncture technique.ing proper sterile technique, remove the Reprocessed ViewFlex Xtra ICE Catheter from the package andplace i t in a sterile work area.10.Carefully inspect the catheter for tip integrity and catheter condition. Do not use the catheter if any damage isnoted. Return the Reprocessed ViewFlex Xtra ICE Catheter and packaging to Stryker if it is not in acceptable condition for the procedure.11.Connect the Reprocessed ViewFlex Xtra ICE Catheter connector edge to the ViewFlex Catheter InterfaceModule. Refer to the ViewFlex Catheter Interface Module Instructions for Use for additionalinstructions, precautions, and information on catheter connection.12.Prior to insertion, test that the catheter is imaging by placing the tip in sterile fluid. Movement willappear on the ultrasound console monitor.13.Hold the catheter 1 to 2 cm from the introducer valve and feed it into the introducer slowly to preventbuckling of t he catheter tip.14.Gently insert the catheter into the selected vein and advance the catheter into the heart. Confirm catheterposition with the use of fluoroscopy, if needed. Do not remove and re-insert the catheter into the introducer more than two (2) times during the procedure.15.The Reprocessed ViewFlex Xtra ICE Catheter tip may be deflected as desired during the procedure:▪For Posterior – Anterior deflection, rotate the gray deflection knob labeled P/A clockwise or counterclockwise▪For Left – Right deflection, rotate the green deflection knob labeled L/R clockwise or counterclockwise16.The catheter handle should be secure at all times during the procedure. Do not allow the catheter handle orconnection cable to fall or tug on the catheter body.NOTE: Do not leave the catheter in the patient longer than 12 hours. Transducer performance or incidence of insertion site complications increase significantly with catheters which remain in dwelling longer than this specified time.17.Return both knobs to the neutral position to straighten the distal tip of the catheter before removing thecatheter from the heart. Using fluoroscopy, verify that the distal tip of the catheter is straightened beforeremoving the catheter f rom the heart.18.Refer to the ultrasound console Users’ Manual for additional sonography instructions, precautions, andinformation on catheter connection.Storage and handling▪Room Temperature: 18°C to +26°C (64°F to 79°F)▪Use product on a first-in, first-out basis prior to expiration or use by date on the labelTransport▪Temperature: -20°C to +50°C (-4°F to 122°F)▪Relative Humidity: 25% to 90%Standards and IEC ClassificationsThe Reprocessed ViewFlex Xtra ICE Catheter meets all pertinent clauses of IEC 60601-1 Edition 3+A1;A2, IEC 60601-1-2 Edition 4.0, and IEC 60601-2-37 Edition 2.1.If the Reprocessed ViewFlex Xtra ICE Catheter experiences loss or degradation of the essential performance described in these instructions as a result of EMC disturbances, there would be no effect to intended use.The medical device is suitable to be used in the Professional Healthcare Facility Environment. WarrantyReprocessed productsStryker warrants all reprocessed products, subject to the exceptions provided herein, to be free from defects in reprocessing and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for one use in accordance with the instructions for use of such product.Products for which Stryker is the original manufacturerStryker warrants all products for which it is the original manufacturer, subject to the exceptions provided herein, to be free from defects in design, materials and workmanship and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for a period of one year from the date of purchase.General warranty terms applicable to all productsTo the fullest extent permitted by law, the express warranty set forth herein is the only warranty applicable to the products and is expressly in lieu of any other warranty by Stryker, expressed or implied, including, but not limited to, any implied warranty or merchantability or fitness for a particular purpose. In no event will Stryker’s liability arising in connection with the sale of the product (whether under the theories of breach of contract, tort, misrepresentation, fraud, warranty, negligence, strict liability or any other theory of law) exceed the purchase price, current market value or residual value of the products, whichever is less. Stryker shall not be liable for indirect, special, incidental, punitive, or consequential damages resulting from any breach of warranty or under any other legal theory.This warranty shall apply only to the original end-user purchaser of products directly from Stryker or a Stryker authorized distributor. This warranty may not be transferred or assigned without the express written consent of Stryker.This warranty does not apply to: (1) products that have been misused, neglected, modified, altered, adjusted, tampered with, improperly installed or refurbished; (2) products that have been repaired by any person other than Stryker personnel without the prior written consent of Stryker; (3) products that have been subjected to unusual stress or have not been maintained in accordance with the instructions in the user manual or as demonstrated by a Stryker representative; (4) products on which any original serial numbers or other identification marks have been removed or destroyed; or (5) products that have been repaired with any unauthorized or non-Stryker components.If a valid warranty claim is received within thirty (30) days of the expiration of the applicable warranty period, Stryker will, in its sole discretion: (1) replace the product at no charge with a product that is at least functionally equivalent to the original product or (2) refund the purchase price of the product. If a refund is provided by Stryker, the product for which the refund is provided must be returned to Stryker and will become Stryker’s property. In any event, Stryker’s liability for breach of warranty shall be limited to the replacement value of the defective or non-conforming part or component.If Stryker determines in its reasonable discretion that the claimed defect or non-conformance in the product is excluded from warranty coverage as described hereunder, it will notify the customer of such determination and will provide an estimate of the cost of repair of the product. In such an event, any repair would be performed at Stryker’s standard rates.Products and product components repaired or replaced under this warranty continue to be warranted as described herein during the initial applicable warranty period or, if the initial warranty period has expired by the time the product is repaired or replaced, for thirty (30) days after delivery of the repaired or replaced product. When a product or component is replaced, the item provided in replacement will be the customer’s property and the replaced item will be Stryker’s property. If a refund is provided by Stryker, the product for which the refund is provided must be returned to Stryker and will become Stryker’s property.ViewFlex and ViewMate are trademarks of St. Jude Medical, Inc.ICE EL10105 Rev. E 07/2023 RM705008。

©2016 Whelen Engineering Company Inc.Form No.14961 (010816)A u t o m o t i v e : For warranty information regarding this product, visit /warranty•Proper installation of this product requires the installer to have a good understanding of automotive electronics, systems and procedures.•Whelen Engineering requires the use of waterproof butt splices and/or connectors if that connector could be exposed to moisture.•Any holes, either created or utilized by this product, should be made both air- and watertight using a sealant recommended by your vehicle manufacturer.•Failure to use specified installation parts and/or hardware will void the product warranty.•If mounting this product requires drilling holes, the installer MUST be sure that no vehicle components or other vital parts could be damaged by the drilling process. Check both sides of the mounting surface before drilling begins. Also de-burr the holes and remove any metal shards or remnants. Install grommets into all wire passage holes.•If this manual states that this product may be mounted with suction cups, magnets, tape or Velcro®, clean the mounting surface with a 50/50 mix of isopropyl alcohol and water and dry thoroughly.•Do not install this product or route any wires in the deployment area of your air bag. Equipment mounted or located in the air bag deployment area will damage or reduce the effectiveness of the air bag, or become a projectile that could cause serious personal injury or death. Refer to your vehicle owner’s manual for the air bag deployment area. The User/Installer assumes full responsibility to determine proper mounting location, based on providing ultimate safety to all passengers inside the vehicle.•For this product to operate at optimum efficiency, a good electrical connection to chassis ground must be made. The recommendedprocedure requires the product ground wire to be connected directly to the NEGATIVE (-) battery post (this does not include products that use cigar power cords).•If this product uses a remote device for activation or control, make sure that this device is located in an area that allows both the vehicle and the device to be operated safely in any driving condition.•Do not attempt to activate or control this device in a hazardous driving situation.•This product contains either strobe light(s), halogen light(s), high-intensity LEDs or a combination of these lights. Do not stare directly into these lights. Momentary blindness and/or eye damage could result.•Use only soap and water to clean the outer lens. Use of other chemicals could result in premature lens cracking (crazing) and discoloration. Lenses in this condition have significantly reduced effectiveness and should be replaced immediately. Inspect and operate this product regularly to confirm its proper operation and mounting condition. Do not use a pressure washer to clean this product.•It is recommended that these instructions be stored in a safe place and referred to when performing maintenance and/or reinstallation of this product.•FAILURE TO FOLLOW THESE SAFETY PRECAUTIONS AND INSTRUCTIONS COULD RESULT IN DAMAGE TO THE PRODUCT OR VEHICLE AND/OR SERIOUS INJURY TO YOU AND YOUR PASSENGERS!Warnings to InstallersWhelen’s emergency vehicle warning devices must be properly mounted and wired in order to be effective and safe. Read and follow all of Whelen’s written instructions when installing or using this device. Emergency vehicles are often operated under high speed stressful conditions which must be accounted for when installing all emergency warning devices. Controls should be placed within convenient reach of the operator so that they can operate the system without taking their eyes off the roadway. Emergency warning devices can require high electrical voltages and/or currents. Properly protect and use caution around live electrical connections.Grounding or shorting of electrical connections can cause high current arcing, which can cause personal injury and/or vehicle damage, including fire. Many electronic devices used in emergency vehicles can create or be affected by electromagnetic interference. Therefore, after installation of any electronic device it is necessary to test all electronic equipment simultaneously to insure that they operate free of interference from other components within the vehicle. Never power emergency warning equipment from the same circuit or share the same grounding circuit with radio communication equipment. All devices should be mounted in accordance with the manufacturer’s instructions and securely fastened to vehicle elements of sufficient strength to withstand the forces applied to the device. Driver and/or passenger air bags (SRS) will affect the way equipment should be mounted. This device should be mounted by permanent installation and within the zones specified by the vehicle manufacturer, if any. Any device mounted in the deployment area of an air bag will damage or reduce the effectiveness of the air bag and may damage or dislodge the device. Installer must be sure that this device, its mounting hardware and electrical supply wiring does not interfere with the air bag or the SRS wiring or sensors. Mounting the unit inside the vehicle by a method other than permanent installation is not recommended as unit may become dislodged during swerving; sudden braking or collision. Failure to follow instructions can result in personal injury. Whelen assumes no liability for any loss resulting from the use of this warning device. PROPER INSTALLATION COMBINED WITH OPERATOR TRAINING IN THE PROPER USE OF EMERGENCY WARNING DEVICES IS ESSENTIAL TO INSURE THE SAFETY OF EMERGENCY PERSONNEL AND THE PUBLIC.Warnings to UsersWhelen’s emergency vehicle warning devices are intended to alert other operators and pedestrians to the presence and operation of emergency vehicles and personnel. However, the use of this or any other Whelen emergency warning device does not guarantee that you will have the right-of-way or that other drivers and pedestrians will properly heed an emergency warning signal. Never assume you have the right-of-way. It is your responsibility to proceed safely before entering an intersection, driving against traffic, responding at a high rate of speed, or walking on or around traffic lanes. Emergency vehicle warning devices should be tested on a daily basis to ensure that they operate properly. When in actual use, the operator must ensure that both visual and audible warnings are not blocked by vehicle components (i.e.: open trunks or compartment doors), people, vehicles, or other obstructions. It is the user’s responsibility to understand and obey all laws regarding emergency warning devices. The user should be familiar with all applicable laws and regulations prior to the use of any emergency vehicle warning device. Whelen’s audible warning devices are designed to project sound in a forward direction away from the vehicle occupants. However, because sustained periodic exposure to loud sounds can cause hearing loss, all audible warning devices should be installed and operated in accordance with the standards established by the National Fire Protection Association.Safety FirstThis document provides all the necessary information to allow your Whelen product to be properly and safely installed. Before beginning the installation and/or operation of your new product, the installation technician and operator must read this manual completely. Important information is contained herein that could prevent serious injury or damage.WARNING: This product can expose you to chemicals including Methylene Chloride which is known to the State of California to cause cancer, and Bisphenol A, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to .Installation Guide:Legacy® R65 WeCan® Lightbar51 Winthrop RoadChester, Connecticut 06412-0684Phone: (860) 526-9504Internet: Salese-mail:*******************CustomerServicee-mail:*******************®ENGINEERING COMPANY INC.IMPORTANT! The lightbar must be a minimum of 16" from any radio antennas.NOTE: There may be a roof support member that spans the distance between the driver’s and passengers side. DO NOT DRILL THROUGH THIS MEMBER! Adjust the location until the holes can be drilled without contacting this support member.Strap Mounting:1.Install the mounting bracket to the mounting foot using the supplied5/16 FLAT WASHERS and 5/16 - 18 ELASTIC STOP NUTS (Fig. 1).Do NOT install the optional spacers yet.2.Place the bracket into the track on the bottom of the extruded base ofthe lightbar and twist it into position (Fig. 2).Permanent Mounting:Caution:Permanent mounting of this product will require drilling.It is absolutely necessary to make sure that no other vehicle components could be damaged by this process. Check both sides of the mounting surface before starting. If damage is likely, select a different mounting location.1.Install the mounting foot to the lightbar following steps 1 thru 4 of “Strap Mounting”.2.Position the lightbar onto the vehicle in its exact mounting location and mark the location of the mounting holes onto the mounting surface using the mounting feet as templates.If the permanent mounting holes in the mounting feet are difficult to access, you can use the measurements shown here to mark off and drill the mounting holes. You will also need to measure the distance between the mounting feet for your application since lightbar width will depend on the lightbar you are mounting.3.Remove the lightbar and drill the 4 mounting holes.4.Install the lightbar using the supplied 1/4 - 20 Phillips Pan Head Metal Screw, 1/4” Internal Tooth Lock Washer and 1/4 - 20 X 7/16 Hex Nut.IMPORTANT! It is the responsibility of the installation technician to make sure that the installation and operation of this product will not interfere with or compromise the operation or efficiency of any vehicle equipment! Before returning the vehicle to active service,visually confirm the proper operation of this product, as well as all vehicle components/equipment.RED = (+) POSITIVE BLACK = (-) NEGATIVEGREEN = COMUNICATIONSGREY = COMUNICATIONS1312LIGHTHEAD OPTIONSHALF TIR TAKEDOWNFULL TIR TAKEDOWNTIR ALLEY LIGHT01-0688130-__R65 WC LEGACY LIGHTBAR, BLUE/AMB 48"01-0688130-__01-0688130-__11-387277-044BASE, EXTRUDED 44.4" MACHINED LOW PROFILE LTBAR 11-387385-050R65 WC LEGACY LIGHTBAR, BLUE/AMB 54"R65 WC LEGACY LIGHTBAR, BLUE/AMB 59"11-387385-0551GROMMET, SPECIAL TO BE MOLDED 1.562"21-11245004-11PLUG, VENT.750 DIA HOLE LIGHTBAR21-7263998-002BRACKET, BULKHEAD LENS MOUNT LOW PROFILE LIGHTBAR 07-26D 863-0006INSULATOR, I.O./EXTRUSION DIE CUT PLASTIC LPL 38-0244488-002ASSY, PCB I/O BOARD LEGACY LTBAR02-0187275-001ASSY,CABLE INPUT 2/C 10 GA 17' LEGACY SOLO 46-0747027-171ASS'Y, CABLE 2/C 20 GA 17' STRIP 1.75"/770904 SCKT 46-0743442-021CABLE CLAMP, 1/2"D, 1/2"W .203" MTG HOLE, BLACK 26-0115037-081NUT, 10-24 CAD PLATED WHIZ OR STEEL ZINC PLATED 13-104111-0631TY WRAP, 6" BLACK26-0215001-061ASSY, CORNER L-FRONT/R-REAR BA R65 LEGACY 01-026G 753-21ASSY, CORNER R-FRONT/L-REAR BA R65 LEGACY 01-026G 754-21BRACKET, I/O ANCHOR LOW PROFILE LIGHTBAR 07-26D 865-000SUB ASSY, FULL TIR TAKE-DOWN LEGACY 01-026E 388-30SUB ASSY, HALF TIR TAKE-DOWN LEGACY01-0246796-30BRACKET, CLAMP SUPPORT HALF DIRECTIONAL LEGACY 07-244477-000SCREW, 6-32 X 1/2 PPHMS SEMS W/IT LOCK WASHER 14-062216-081BASE, MACHINED 50.228" LEGACY LIGHTBAR 1SCREW, 10-24 X .875"TX PHD SWEDGE FORM 1/4" LEAD 5/8"THD 14-0023347-01R65 WC LEGACY LIGHTBAR, BLUE/AMB, 44"01-0688130-__221A/R 28BASE, EXTRUDED 39.62"" MACHINED LOW PROFILE LTBAR 11-387277-039BASE, MACHINED 55.008" LEGACY LIGHTBAR 221A/R A/R26112421111111A/R11242111111221A/R A/R 261A/R 11262111111221A/R A/R 281A/R A/R SUB ASSY,ALLEY LIGHT LEGACY 01-0244498-3023ITEMPART NUMBERDESCRIPTIONQTY QTY QTY QTY 11121314151617181920456789101212223BRACKET, SNAP-IN LT MODULE MT LOW PROFILE LIGHTBAR07-26D 864-000ASSY, HARNESS "A" LP LIGHTBAR46-0787374-01ASSY, HARNESS "E" LP LIGHTBAR 46-0787374-00ASSY, HARNESS "F" LP LIGHTBAR 46-0787374-05ASSY, HARNESS "E" 55" LEGACY 46-0787395-00SUB ASSY, FULL LENS, CLEAR, LEGACY LIGHTBAR 02-036E 690-30COVER,TOP EXTRUDED 21.665" MACHINED LO PRO LTBAR 11-26E 056-021COVER,TOP CENTER11-26E 377-009SEAL, LENS DIVIDER LOW PROFILE LED LIGHTBAR 38-046D 854-00DIVIDER, LENS LOW PROFILE LED LIGHTBAR 38-046D 853-00SCREW,10 X 7/8T-25TORX TRUSS HD PLASTI-LOC SS W/NYSEAL 15-105C 76-148SUB ASSY, LOW PROFILE MTG FOOT 02-0387331-00LABEL, "FRONT" LIGHTBAR ASSYS 10-0322935-002412214212211LENS, CLEAR CENTER68-196E 376-3011-26E 056-019COVER,TOP EXTRUDED 19.275" MACHINED LO PRO LTBAR A/R TY WRAP, 3" BLACK26-0215001-034SCREW, 10-24 X 1.25" WAX DIP SHOULDER PHTX TRI POINT SS14-104286-16J 110-0526209-00LABEL, MODEL & SERIAL NO, LEGACY 407-223841-000BRACKET, FILLER LEGACY LTBAR ASSY, HARNESS "F" 55" LEGACY 46-0787395-031LABEL, CENTER DOME REMOVAL INSTRUCTIONS10-0346824-0041607-244476-00007-244379-000BRACKET, HALF DIRECTIONAL LEGACY BRACKET, FULL REFLECTOR LEGACY ASSY, HARNESS "E" 59" LEGACY ASSY, HARNESS "F" 59" LEGACY46-0787432-0046-0787432-031102-036E 690130SUB ASSY, CUT LENS, CLEAR, LEGACY LIGHTBAR 101-046E 868-00KIT, UNIVERSAL CONTROL POINT WECAN161112218212A/R 412121201112221821A/R 412412120112142122112A/R 41411161303132333435363738392425262728294041495042434445464748846423822462321404147373639454426261824202017341825171920。

电工翻译词汇L4L grader,L 分级器LaB6 cathode,六硼化镧阴极label,标号labelling,加标laboratory reliability test,实验室可靠性试验laboratory salinometer,实验室盐度计ladder diagram,梯形图lag compensation,滞后补偿76lag module,滞后组件lag network,滞后网络lag-lead compensation,滞后超前补偿Lagrangian method,拉格朗日法Laman spectrophotometer,拉曼分光光度计laminar low,层流laminated glass window,层压玻璃观察窗laminated magnet,积层磁铁landing impact testing machine,落锤式冲击试验机Laplace transform,拉普拉斯变换Laplace-Gauss distribution,拉普拉斯-高斯分布large scale system,大系统large scale system cybernetics,大系统控制论large volume sampler,大容量采水器laser,激光器laser alignment instrument,激光导向仪laser anemometer,激光风速计laser atomizer,激光原子化器laser beam ionization,激光电离laser ceilometer,激光测云仪laser distance meter,激光测距仪laser ellipseness measuring instrument,激光椭圆度测量仪laser fluorescence detector,激光荧光探测仪laser geodynamic satellite（LAGEDS),激光测地卫星laser gravimeter,激光重力仪laser inside diameter measuring instrument,激光内径测量仪laser interferometer,激光干涉仪laser interferometry,激光干涉测量laser length measuring instrument,激光式测长仪laser level,激光水准仪laser microspectral analyzer,激光显微光谱分析仪laser orientation instrument,激光指向仪laser outside diameter measuring instrument,激光外径测量仪laser plummet,激光垂准仪laser printer,激光印刷机laser probe mass spectrometer,激光探针质谱计laser scatterometer,激光散射计laser sensor,激光传感器laser spectrum radiator,激光光谱辐射计laser tachometer,激光转速仪laser theodolite,激光经纬仪latent heat,潜热lateral logger,侧向测井仪lateral probe movement,左右扫查77lateral scan,左右扫查lead capacitance,接线电容lead compensation,超前补偿lead inductance,接线电感lead/lag module,超前/滞后组件lead module,超前组件lead network,超前网络leading edge,前缘leading peak,前伸峰leak pressure,泄漏压力leakage current screen,泄漏电流屏蔽leakage magnetic field,漏磁场leakage magnetic field inspection,漏磁探伤法leakage magnetic flow detector,漏磁探伤仪leakage resistance,漏电阻least-squares line,最小二乘直线least-squares linearity,最小二乘线性度length,长度 length control device,定长装置length of a scale division,标度分格间距；分格（度）长度lengthy bellows,长波纹管lens micrometer,透镜测微器level,水准仪；水准器；水准泡；级；电平；物位level recorder,电平记录仪level transducer(sensor),物位传感器leve-braked motor,杠杆式制动电动机lever-type vibrograph,杠杆式测振仪library,程序库。