Operators Manual
58 Pages
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FLUID MANAGEMENT SYSTEM Operator’s Manual
Fluent Fluid Management System Operator’s Manual
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Fluent Fluid Management System Operator’s Manual
Procedure Setup: Introduction... 6 Chapter 1: Introduction to Fluent Fluid Management System... 11 Chapter 2: Configuring the Touchscreen Settings... 17 Chapter 3: Connecting the System Components ... 18 Chapter 4: Priming the System... 24
During Procedure: Chapter 5: Operating the System... 25 Chapter 6: Replacing Components... 27
After Procedure: Chapter 7: Disassembly and Disposal... 30 Chapter 8: Maintenance... 32
Troubleshooting Chapter 9: Notifications and Messages... 34 Chapter 10: Troubleshooting... 36
Supplementary Information Chapter 11: Annual Inspection and Testing... 42 Chapter 12: Technical Specifications... 43 Chapter 13: Electromagnetic Compatibility... 45 Chapter 14: Disposables and Accessories... 48 Chapter 15: Service and Warranty Information... 49 Symbols... 51 Glossary... 54
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Procedure Setup
Fluent Fluid Management System
Introduction This manual is written for medical personnel who will be responsible for operating the Fluent® Fluid Management System. It is extremely important that the operator read and thoroughly understand the contents of this manual, and follow the instructions contained herein for reliable, safe and efficient operation of the product. RX ONLY (U.S.) Federal law restricts this device to sale by or on the order of a physician pursuant to 21 CFR 801.109(b)(1).
Copyright/Trademark Information Hologic and Fluent are registered trademarks of Hologic, Inc. and its subsidiaries in the United States and other countries. All other trademarks, registered trademarks, and product names are the property of their respective owners.
Manufacturer HOLOGIC, INC. 250 Campus Drive, Marlborough, MA 01752 USA 1.800.442.9892 (US Toll Free)
Indications For Use The Fluent Fluid Management System is intended to provide liquid distension of the uterus during diagnostic and operative hysteroscopy, and to monitor the volume differential between the irrigation fluid flowing into and out of the uterus while providing drive, control and suction for hysteroscopic morcellators.
Intended Use The Fluent® Fluid Management System is intended to provide liquid distension of the uterus during diagnostic and operative hysteroscopy, and to monitor the volume differential between the irrigation fluid flowing into and out of the uterus. The Fluent Fluid Management System is designed to be used in operating room, ambulatory surgical center, and physician’s office environments. The gynecologist should be trained in diagnostic and therapeutic hysteroscopy, resection, and removal of gynecological tissue.
Contraindications The system may not be used to introduce fluids into the uterus when hysteroscopy is contraindicated. See the operator’s manual of your hysteroscope for absolute and relative contraindications. The Fluent Fluid Management System should not be used to remove pathologies from pregnant patients or patients exhibiting pelvic infection, cervical malignancies, or previously diagnosed endometrial cancer. Relative contraindications to endometrial ablation: Hysteroscopic endometrial ablation, whether by laser or electrosurgery, should not be undertaken before adequate training, preceptorship, and clinical experience. Additionally, tissue sampling is required prior to destruction of the endometrium. The following are clinical conditions that can significantly complicate hysteroscopic endometrial ablation: • Adenomatous endometrial hyperplasia • Uterine leiomyoma • Severe adenomyosis • Pelvic pain (subtle PID) • Uterine anomalies • Surgical skill (see above) • Severe anemia • Inability to circumnavigate the myoma (re: myoma size) - predominantly intramural myomas with small submucous components.
Important User Notes Read this manual carefully and become familiar with the operation and function of the Fluent Fluid Management System and the accessories before use during surgical procedures. Non-observance of the instructions listed in this manual can lead to: • Life-threatening injuries to the patient • Severe injuries of the surgical team, nursing staff, or service personnel • Damage or malfunction of the system and/or accessories 6
Introduction
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Fluent Fluid Management System
Essential Performance Essential Performance of the Fluent Fluid Management System is to provide fluid irrigation and monitor fluid use to prevent unacceptable levels of intravasation.
Warnings, Cautions, and Notes Defined The words WARNING, Caution, and Note carry special meanings.
WARNING! Warnings indicate risks to the safety of the patient or user. Failure to follow warnings may result in injury to the patient or user.
Caution! Cautions indicate risks to the equipment. Failure to follow cautions may result in damage to the system or the potential loss of patient data or system data.
Note: Notes provide special information to clarify instructions or present additional information.
Warnings and Precautions The operating instructions in this guide make the system easier to use, while the recommended maintenance procedures help to ensure optimal performance over years of reliable use. As with any surgical instrument, there are important health and safety considerations. These are listed below and highlighted within the text. In order to meet the IEC 60601 safety standard, this console is equipped with an potential equalization conductor which can be used to bring other equipment into the same case potential as the console.
Note: The following warnings and cautions apply only to the Fluent Fluid Management System. For details, warnings, and cautions on using the hysteroscope and tissue removal device with the Fluent Fluid Management System, refer to the specific documentation for the device.
WARNING! • Check all factory settings. • Before using the Fluent Fluid Management System for the first time, please review all available product information. • Before using the Fluent Fluid Management System, you should be experienced in hysteroscopic surgery with powered instruments. Healthy uterine tissue can be injured by improper use of the tissue removal device. Use every available means to avoid such injury. • Use only the Fluent Fluid Management System to connect to the MyoSure® Tissue Removal Device. Use of any other drive mechanism may result in failure of the device to operate or lead to patient or physician injury. • The use of accessory equipment in the patient vicinity not complying with the equivalent medical safety requirements of this equipment may lead to a reduced level of safety of the resulting system. The use of accessory equipment outside the patient vicinity not complying with medical or otherwise appropriate safety requirements may lead to a reduced level of safety of the resulting system. • The use of an accessory, transducer, or cable, other than those specified by Hologic may result in increased emissions or decreased immunity of the Fluent Fluid Management System. • Intrauterine distention is usually possible with pressure values between 35 to 70 mmHg. A pressure above 75 to 80 mmHg is required only in rare cases or if the patient has an excessively high blood pressure. • An air embolism can be the result of air contained in the tube set or connected instrument reaching the patient. Ensure there is always fluid in the bag to prevent air from being pumped into the patient. • Place the system in such a way as to allow for easy visualization of the display values, system functions, and access to the control elements. • Pressing the ON/OFF switch does not disconnect the system from the wall power outlet. This requires pulling the power cord located in the rear of the system. • No modification of this equipment is allowed. • To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective earth. • To avoid risk to patient and operators, do not use this equipment in the presence of intentional magnetic sources, intentional ultrasound sources, or intentional heat sources. • Consult an expert on electromedicine safety before using this equipment near an RF generator to ensure proper setup and use. If you detect or suspect any interference between the Fluent system and any other medical system, discontinue use of the Fluent system and contact customer support. English
Introduction
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Fluent Fluid Management System • Patient and operators are exposed to plastic (tube set, TRD), metal (console, TRD) and fluid (saline). • Do not prime inside the patient. Fluid overload: There is a risk of irrigation fluid reaching the circulatory system of the patient’s soft tissue by passing through the uterus. This can be affected by distention pressure, flow rate, perforation of the uterine cavity and duration of the hysteroscopic surgery. It is critical to closely monitor the input and outflow of the distending liquid at all times. Fluid deficit: The fluid left in the patient must be monitored. The deficit is the total amount of fluid left in the patient or unaccounted for otherwise. Take notice of the measurement tolerance of the system. Estimating the fluid volume remaining in the patient is the physician’s responsibility. Fluid intake and output surveillance: Strict fluid intake and output surveillance should be maintained. If a low viscosity liquid distention medium is used, intrauterine instillation exceeding 2 liters should be followed with great care due to the possibility of fluid overload. If a high viscosity fluid (e. g. Hyskon) is used, the use of more than 500 ml should be followed with great care. See labeling for Hyskon for additional information. Hyponatremia: Some distension fluids may lead to fluid overload and, consequently, hyponatremia with its attending sequelae. This can be affected by the distending pressure, flow rate, and duration of hysteroscopic procedure. It is critical to closely monitor the input volume and outflow volume of the distending liquid at all times. Pulmonary edema: Hysteroscopic surgery is associated with a risk of developing pulmonary edema resulting from fluid overload with isotonic fluids. It is critical to closely monitor the input and outflow of the distending liquid at all times. Cerebral edema: Hysteroscopic surgery is associated with a risk of developing cerebral edema resulting from fluid overload and electrolyte disturbances with hyperosmolar (nonionic) fluids such as glycine 1.5% and sorbitol 3.0%. It is critical to closely monitor the input and outflow of the distending liquid at all times. Idiosyncratic reactions In rare cases, idiosyncratic reactions, including intravascular coagulopathy and allergic reaction including anaphylaxis may occur while performing hysteroscopy if a liquid distention medium is used. Specifically, idiosynatric anaphylactoid reactions have been reported when using Hyskon as an irrigation fluid during hysteroscopy. These should be managed like any allergic reaction. Hypothermia (monitoring body temperature) . ontinuous flow of distention fluids can lead to a lowering of the patient’s body temperature during hysteroscopic surgery. Lower body C temperatures can cause coronary and cardiovascular problems. Always monitor the patient’s body temperature during the entire surgery. Make especially sure that the following, hypothermia promoting, operation conditions are avoided as best as possible: longer operating times and use of cold irrigation fluid. Rupture of the fallopian tube secondary to tubal obstruction Distention of the uterus may lead to a tear of the fallopian tube should there be an obstruction or permanent occlusion. The rupture could lead to irrigation fluid flowing into the patient’s peritoneal cavity, resulting in a fluid overload. It is critical to closely monitor the input and outflow of the distending liquid at all times. Original accessories For your own safety and that of your patient, use only Fluent accessories. Danger: explosion hazard Do not use in the presence of a flammable anesthetic mixture. Do not use in the presence of flammable gases or liquids. Professional qualification This manual does not include descriptions or instructions for surgical procedures/ techniques. It is also not suitable for training physicians in the use of surgical techniques. Medical instruments and systems may be used only by physicians or medical assistants with the appropriate technical/medical qualification working under the direction and supervision of a physician. Sterile media and accessories Always work exclusively with sterile substances and media, sterile fluids, and sterile accessories, if so indicated.
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Fluent Fluid Management System Replacement accessories In case any of the accessories fail during a procedure, replacement accessories should be kept within easy reach to be able to finish the operation with the replacement components. Cleaning the system Do not sterilize the system. Condensation / Water penetration Protect the system from moisture. Do not use if moisture has penetrated the system. System defect If a system defect is suspected or confirmed, do not use the system. Ensure the system is fully functional as described in Chapter 8: Maintenance. Replacing fuse Replace the fuse only with a fuse of the same type and rating. The fuse type is T5AH, 250 V fuses. There are 2 per system. Single Use Tubing sets are single use disposables. Danger: Explosion Hazard Do not use in the presence of an oxygen rich environment. Oxygen Rich Environment is environment in which the concentration of oxygen is: a) greater than 25 % for ambient pressures up to 110 kPa; or b) the partial pressure of oxygen is greater than 27,5 kPa at ambient pressures exceeding 110 kPa
Caution! Electrical Interference: • Electrical interference with other devices or instruments was practically eliminated when developing this system and none was detected during testing. However, if you still detect or suspect such interference, please follow these suggestions: - Move the Fluent Fluid Management System, the other device, or both devices to a different location - Increase the distance between devices used - Consult an electro-medical expert • Do not sterilize or immerse the Fluent Fluid Management System in disinfectant. • Electrical safety testing should be performed by a biomedical engineer or other qualified person. • This equipment contains electronic printed circuit assemblies. At the end of the useful life of the equipment, it should be disposed of in accordance with any applicable national or institutional related policy relating to obsolete electronic equipment. Electromagnetic Safety This section contains important information regarding the electromagnetic safety of this product. • The Fluent Fluid Management System needs special precautions regarding electromagnetic safety and needs to be installed and put into service according to the electromagnetic safety information provided in this manual. • This equipment is designed and tested to minimize interference with other electrical equipment. However, if interference occurs with other equipment it may be corrected by one or more of the following measures: - Reorient or relocate this equipment, the other equipment, or both. - Increase the separation between the pieces of equipment. - Connect the pieces of equipment into different outlets or circuits. - Consult a biomedical engineer. • All equipment performance is considered safety-related performance. That is, the failure or degradation of the performance specified in this manual will pose a safety risk to the patient or operator of this equipment.
Note: If the Fluent Fluid Management System is put into service in accordance to the safety instruction in this manual, the product should remain safe and provide the performance listed above. If the product fails to provide this level of performance, the procedure should be aborted. Contact Hologic. The problem needs to be corrected before continuing or starting a new procedure.
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Introduction
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Fluent Fluid Management System • Portable and mobile RF communications equipment, including cellular telephones and other wireless devices, can affect medical electrical equipment. To insure safe operation of the Fluent Fluid Management System, do not operate communications equipment or cellular telephones at a distance closer than specified in Chapter 13: Electromagnetic Compatibility. • The Fluent Fluid Management System is not designed to work with or in the vicinity of electrical surgical equipment. If electrical surgical equipment must be used in the same area as the Fluent Fluid Management System, the Fluent Fluid Management System should be observed for proper operation before performing a procedure. This includes operating the electrical surgical equipment in its active mode at a power level suitable for the procedure. • Use of the Fluent Fluid Management System adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, the Fluent Fluid Management System and the other equipment should be observed to verify that they are operating normally. • For more information regarding the electromagnetic safety of this product, please see Chapter 13: Electromagnetic Compatibility.
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Introduction
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Fluent Fluid Management System
Chapter 1: Introduction to Fluent Fluid Management System This chapter introduces the Fluent Fluid Management System by describing all the components for use.
Introduction to the Fluent Fluid Management System The Fluent Fluid Management System (FMS) is designed to provide liquid distension of the uterus during diagnostic and operative hysteroscopy while monitoring the volume differentials between fluid flowing into and out of the uterus. Additionally, the Fluent Fluid Management System supports the use of the MyoSure Tissue Removal Devices for tissue removal. Technical application scope of the system The Fluent Fluid Management System allows intrauterine pressure to be adjusted between 40 and 120 mmHg. The maximum inflow rate is 650 ml/min and is reduced automatically by the pump once the pre-set intrauterine pressure setting has been reached. The system has been designed to provide both fluid and vacuum systems that maximize the performance of the MyoSure® Tissue Removal System. Suggested distension media The Fluent Fluid Management System should only be used with Sterile Media. The Fluent Fluid Management System can be used with hypotonic, electrolyte-free media (e.g., glycine 1.5% and sorbitol 3.0%) and isotonic, electrolyte containing media (e.g., saline 0.9% and Lactated Ringer’s). See “Introduction” section for risks related to Viscosity and the use of a high viscosity media such as Hyskon under “Fluid intake and output surveillance.” Pressure measuring and regulating The system operates with a completely non-contact pressure measurement of the irrigation medium. The pressure control circuit continuously compares the desired preset intrauterine pressure with the actual intrauterine pressure. The function of this algorithm is to maintain the pre-set intrauterine pressure. Components Included With the Fluent Fluid Management System This section lists and describes the Fluent Fluid Management System components. 1 1
Fluid Bag Hooks
Location to hang up to 6L of fluid
2
Fluid Bag Pole
Contains two IV Hooks to hang up to 6L fluid
3
Touchscreen Monitor
Allows configuring, adjusting, and monitoring the status
4
Fluent In-FloPak Receptacle
Location to insert the Fluent In-FloPak
5
Fluent Out-FloPak Receptacle
Location to insert the Fluent Out-FloPak
6
MyoSure Tissue Removal Device (TRD) Connector
Location to connect the MyoSure TRD drive cable to the Fluent Fluid Management System
7
Foot Pedal Connector
Location to connect the MyoSure Foot Pedal cord to the Fluent Fluid Management System
8
Waste Bag Hanger Location to hang a Waste Bag
9
Waste Bag
2
3
4
5
6 7
8
Waste Bag
10 Wheels
Enables movement and positioning of the Fluent Fluid Management System
11 Wheel Locks
Prevents movement and positioning of the wheels
9
10 11 Figure 1: The front of the Fluid Management System console with corresponding component parts attached
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Chapter 1: Introduction to Fluent Fluid Management System
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Fluent Fluid Management System The following illustration shows the components on the rear of the Fluent Fluid Management System console. 12
Handle
-G rasp to move and position the System - L ocation to wrap the Power Cord when not in use
13
On/Off Switch
Turns the System On (|) and Off (O)
14
Power Port
Location to connect the Power Cord to the System
15
Equipotential Plug
Connector used to electrically bond the system to another conductive material, or ground the system to a safety ground.
16
Storage Basket mount points
12 15
14 13
16
Location to hang Storage Basket
Figure 2: The rear of the Fluent Fluid Management System console The shipping crate contains the Fluent Fluid Management System console and a separate shipping box containing the Fluent Fluid Management System components. The following components are contained in the Fluent Fluid Management System shipping box: • Foot Pedal: Controls MyoSure Tissue Removal Device (TRD) operation • Storage Basket: Container for lightweight items such as the Foot Pedal when not in use • Power Cord: Establishes an electrical connection between the Fluent Fluid Management System and a wall outlet • Fluent Fluid Management System Initial Setup Card: One sheet that shows how to unpack and set up the Fluent Fluid Management System • Fluent Fluid Management System Operator’s Manual: Document that describes how to use the Fluent Fluid Management System • Fluent Fluid Management System User Reference Card: One sheet that highlights how to use the Fluent Fluid Management System For a list of components not included, see Chapter 14: Disposables and Accessories
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Chapter 1: Introduction to Fluent Fluid Management System
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Fluent Fluid Management System Fluid Bag Fluid Bags (not included) hang on the IV Hooks at the top of the Fluent Fluid Management System. Hooks provide the ability to hang up to 6 liters of fluid containing hypotonic, isotonic, ionic and non-ionic distention fluids at once. The Fluid Bag Tube connects to the blue Inflow Tube Set, which connects to the hysteroscope Inflow Channel Tube. Fluid is pulled from the Fluid Bag through the Inflow Tube Set and delivered through the hysteroscope Inflow Channel Tube into the patient’s uterus.
WARNING! Placing excessive force or weight on the IV Hooks can overload the scale connected to the IV Hooks. Doing so may result in an inaccurate fluid deficit value, causing risk to patient safety.
WARNING! When performing monopolar hysteroscopic electrosurgery, the distension medium must be electrically non-conductive. Examples include glycine, sorbitol and mannitol. Isotonic irrigation fluids may only be used when performing bipolar electrosurgical resection procedures. Examples include saline and lactated Ringer’s solution. Touchscreen Monitor The Touchscreen Monitor includes two system speakers and the Touchscreen User Interface. Tilt and swivel the monitor for optimal viewing.
Caution! Only use the Handle to move or position the Fluent Fluid Management System. Do not pull or push the system by the Touchscreen Monitor. Touchscreen User Interface Use the Touchscreen User Interface to configure and view system information, set the deficit limit, prime the system, and make other adjustments as needed. The Touchscreen prompts performing a task (such as Hang Fluid Bag) and displays task status (such as Fluid Bag Hung). Touchscreen Icons Icon
English
Name
Description
Help
Displays additional information
System Settings
Displays the System Settings screen
Clear
Clears an error condition once the user has taken steps to resolve the issue
Back
Displays the previous screen
Next
Displays the next step or screen
Prime
Primes the system
Pause
Pauses the procedure. When the system is paused, this button changes to Run to restart the procedure.
Change
Displays the available settings for the selected item
Down/Up
Decreases or increases the settings for the selected item
Accept/Confirm
Applies the change to the selected setting
Cancel/Decline
Cancels the change to the selected setting
Chapter 1: Introduction to Fluent Fluid Management System
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Fluent Fluid Management System
Run
Starts the pumps running to provide irrigation. When running, this button changes to Pause to halt the pumps.
Complete Procedure
When ending a procedure, the Outflow pump continues to run to collect the remaining flow. Pressing this button stops the Outflow pump and displays the values for Total Deficit, Total Fluid Volume, Final Pressure, and Cutting Time.
Exit
Returns to previous screen
New Procedure
Displays the System Setup screen to start a new procedure
Last Procedure
Displays results from the previous procedure
Load Cell Calibration Check
Opens the utility for checking the calibration of the supply and waste scales. Refer to Ch.11 for instructions on how to perform the Load Cell Calibration Check.
Pressure Calibration Check
Opens the utility for checking the calibration of the pressure sensor. Refer to Ch. 11 for instructions on how to perform the Pressure Calibration Check.
Software Update
Opens the utility for performing system software updates. This utility is intended for use by Hologic personnel only.
End
Ends the procedure and begins evacuating the Out-FloPak tubing
Zero
Resets the procedure’s deficit value to zero
Reprime
Primes the system again after a procedure has started
Done
Ends evacuation of the Out-FloPak tubing
Fluent Procedure Kit The Fluent Procedure Kit contains the Fluent In-FloPak, the Fluent Out-FloPak, the Waste Bag, and the Tissue Trap.
WARNING! Do not reprocess of sterile disposable products Reuse of Fluent In-FloPaks or Fluent Out-FloPaks can cause an infection hazard for patients and/or users as well as impair product functionality. Contamination and/or impaired functionality of the system can cause risk of injury, illness, or death. Do not re-process any of the components contained within the single-use Procedure Kit. Fluent In-FloPak The blue Fluent In-FloPak pulls clean fluid from the Fluid Bag. The Fluent In-FloPak contains the Fluid Bag Tube and the hysteroscope Inflow Tube. It fits securely into the blue Fluent In-FloPak Receptacle on the front left side of the Fluid Management System. Before each procedure, connect the tubes as follows:
Fluent In-FloPak
• From the Fluid Bag Tube spike to the Fluid Bag • From the hysteroscope Inflow Tube (that has a blue band adjacent to the Luer lock connector) to the Hysteroscope Inflow Channel These connections allow the transfer of irrigation fluid from a Fluid Bag to the hysteroscope Inflow Channel. The flow of fluid is monitored and controlled using the Touchscreen to maintain the pressure at a specified setting.
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Chapter 1: Introduction to Fluent Fluid Management System
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Fluent Fluid Management System Fluent Out-FloPak The yellow Fluent Out-FloPak drains waste fluid from the hysteroscope Outflow Channel, the MyoSure Tissue Removal Device (TRD) Tube, and the Under Buttocks (UB) Drape Tube into the Waste Bag. The Fluent Out-FloPak contains the Waste Bag Tube (which contains the in-line Tissue Trap), the hysteroscope Outflow Tube, the MyoSure Tissue Removal Device (TRD) Tube, and the Under Buttocks (UB) Drape Tube. It fits securely into the yellow Fluent Out-FloPak Receptacle on the front right side of the Fluid Management System. Before each procedure, connect the tubes as follows: • From the Waste Tube connector to the Waste Bag • From the hysteroscope Outflow Tube (that has a yellow band adjacent to the Luer lock connector) to the Hysteroscope Outflow Channel • Only when using MyoSure Tissue Removal Device (TRD) connect the tube that has a green band adjacent to the barb connector to the MyoSure Tissue Removal Device (TRD)
Fluent Out-FloPak • From the Under Buttocks (UB) Drape Tube (that has a yellow suction connector) to the Under Buttocks (UB) Drape Port These connections allow the transfer of fluid from the hysteroscope Outflow Channel, the MyoSure Tissue Removal Device (TRD), and the Under Buttocks (UB) Drape Port to the Waste Bag. Waste Bag The Waste Bag is designed to capture waste fluid from hysteroscopic procedures. The Waste Bag hangs on the Waste Bag Hanger at the bottom of the Fluent Fluid Management System. Hang only one Waste Bag at a time. The Waste Bag includes an attached cap. For details on replacing the Waste Bag, see Chapter 6: Replacing Components. If an accurate manual deficit assessment is required, pour fluid into calibrated container.
.WARNING! The markings on the waste bag are not intended as a measuring device, only for general reference, not a specific volumetric measurement.
Waste Bag Tissue Trap The Waste Tube contains an in-line Tissue Trap designed to capture resected tissue throughout the procedure to allow the tissue to be sent to pathology for testing. The Tissue Trap Holder contains the Tissue Trap that captures the resected tissue. Please monitor the Tissue Trap so it does not overfill. For details on handling the Tissue Trap, see Chapter 7: Disassembly and Disposal.
Tissue Trap
Controls and Functions This section describes Fluent Fluid Management System controls and functions. Wheels
The four wheels located on the bottom of the Fluent Fluid Management System enable movement and positioning of the Fluent Fluid Management System. For details on using the Wheel Locks, see Assembly Instructions provided in Chapter 3.
Contained in the Shipping Box Foot Pedal The Foot Pedal controls tissue removal device operation. It connects to the Foot Pedal Connector located on the Fluent Fluid Management System front panel. English
Chapter 1: Introduction to Fluent Fluid Management System
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Fluent Fluid Management System Storage Basket The Storage Basket hangs on the rear of the Fluent Fluid Management System. It is used to store lightweight items such as the Foot Pedal when not in use. Do not place heavy items in the Storage Basket. The maximum recommended weight is 10 pounds. Power Cord The Power Cord connects to Power Cord Connector located on the rear of the Fluent Fluid Management System. When the system is not in use, wrap the Power Cord around the Handle on the rear of the system.
Located on the Front of the Fluent Fluid Management System MyoSure Tissue Removal Device (TRD) Connector The MyoSure Tissue Removal Device (TRD) Connector is located on the Fluent Fluid Management System front panel above the Foot Pedal Connector. For details on operating the Tissue Removal Device, refer to MyoSure Tissue Removal Device Instructions For Use. Foot Pedal Connector The Foot Pedal Connector is located on the Fluent Fluid Management System front panel below the MyoSure Tissue Removal Device (TRD) Connector. Foot Pedal Connector
Located on the Rear of the Fluent Fluid Management System Handle The Handle is located on the rear of the system.
Caution! Only use the Handle to move or position the Fluent Fluid Management System. Do not pull or push the system by the IV Hooks or the Touchscreen Monitor. On/Off Switch The On/Off Switch is located on the rear of the Fluent Fluid Management System above the Power Cord Connector. The On/Off Switch is labeled with | for On and O for Off. Power Cord Connector The Power Cord Connector is located on the rear of the Fluent Fluid Management System below the On/Off Switch. Equipotential Plug
Rear of System
The connector used to electrically bond the system to another conductive material, or ground the system to a safety ground. After you have been introduced to the Fluent Fluid Management System components, you are ready to learn how to configure the Touchscreen settings. The next chapter describes configuring the Touchscreen settings.
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Chapter 1: Introduction to Fluent Fluid Management System
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Fluent Fluid Management System
Chapter 2: Configuring the Touchscreen Settings After you have been introduced to the Fluent Fluid Management System components, you are ready to configure the Touchscreen settings. This chapter describes how to configure the Touchscreen settings.
Turning on the Fluent Fluid Management System WARNING! To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective earth. WARNING! Equipment should be positioned such that power cord can be easily disconnected. To turn the system on, perform the following steps. 1. Connect the Power Cord to the rear of the Fluent Fluid Management System. 2..Plug the Power Cord directly into a wall outlet with the appropriate power for the Fluent Fluid Management System. 3. Press the top of the On/Off switch on the rear of the system to the On (|) position. The system performs a setup routine and then displays the System Setup screen (Screen 1).
Screen 1: System Setup Screen
Note: Touch the Help icon ( ) at any time to display step-by-step instructions on the touchscreen.
Configuring the Settings When you first turn on the system, the System Setup screen is displayed. To configure the system settings, touch the Settings icon ( ). The Settings screen is displayed as shown in Screen 2. Use the Settings screen to: • Select the language to display • Adjust the touchscreen brightness • Adjust the speaker volume for alerts • Display additional system information To configure the settings, do any of the following:
Screen 2: Settings Screen
• To configure the Language, touch the down arrow and select the language. • To increase or decrease the Brightness, touch the plus sign or the minus sign. • To increase or decrease the Volume, touch the plus sign or the minus sign. • To view last procedure information, touch Last Procedure. After configuring the Touchscreen settings, you will want to connect the Fluent Fluid Management System components. The next chapter describes connecting the Fluent Fluid Management System components.
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Chapter 2: Configuring the Touchscreen Settings
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Fluent Fluid Management System
Chapter 3: Connecting the System Components After you have configured the Touchscreen settings, you are ready to connect the Fluent Fluid Management System components. This chapter provides information and instructions for moving the system and connecting components.
Note: For details on the setup and operation of the hysteroscope, refer to the hysteroscope’s Instructions For Use.
Before Moving the Fluent Fluid Management System Before moving the system from one location to another, make sure the system is in transport position: • The Power Switch is in the Off (O) position • The Power Cord is unplugged from the mains outlet and wrapped around the Handle on the rear of the system • The Foot Pedal is disconnected from the front of the system and is located in the Storage Basket on rear of the system • The wheels are in the unlocked position • No fluid bags are attached to either the supply or waste hooks • The rear basket contents weigh less than 10 lbs Locking and Unlocking the Wheels All wheels swivel to ease steering and positioning of the system, and have locks, as shown. To lock the wheels: Use your foot to touch down on the outer part of each wheel lock to secure the system from rolling, as shown. To unlock the wheels:
Wheel Lock
Use your foot to touch against (inward) the upper part of each wheel lock.
Using the Handle to Move the Fluent Fluid Management System To move the Fluent Fluid Management System from one location to another, make sure to use only the Handle to push, pull, or steer the system.
WARNING! Placing excessive force or weight on the IV Hooks can overload the scale connected to the IV Hooks. This can result in an inaccurate fluid deficit value, causing risk to patient safety.
Caution! Do not lean on the Handle. Leaning may cause the system to tip.
Positioning the System It is important to position the Fluent Fluid Management System a minimum of 5 ft (1.5 m) from the MyoSure Tissue Removal Device (TRD) to allow the Tissue Removal Device drive cable to hang in a large arc with no bends, loops, or kinks. The ideal placement of the Fluent Fluid Management System is behind the Physician either to the right (if right-handed) or to the left (if lefthanded).
Connecting the Components Connecting the Power Cord The Power Cord is connected to the rear of the system and wrapped around the Handle when not in use. Connect the Power Cord directly into a wall outlet. Make sure the Fluent Fluid Management System is positioned in such a way that the Power Cord does not obstruct positioning or cause a tripping hazard.
WARNING! Equipment should be positioned such that the Power Cord can be easily disconnected.
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Chapter 3: Connecting the System Components
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Fluent Fluid Management System
Caution! Check to ensure the available wall outlet voltage matches the data listed on the label attached to the rear of the system. Incorrect voltage can cause errors and malfunctions and may destroy the system. The power connection must be equipped with a grounding outlet. Use the Fluent Fluid Management System Power Cord to establish a connection between the wall outlet and the Power Port located on the rear of the Fluid Management System.
Note: For more information about power cord safety, see Chapter 12: Technical Specifications.
Identifying Fluent Flo-Pak Tubes Fluent In-FloPak Tubes The tubes of the blue Fluent In-FloPak connect to the following: • The Fluid bag • The Hysteroscope Inflow Channel Fluent Out-FloPak Tubes The tubes of the yellow Fluent Out-FloPak connect to the following: • The Waste Bag • The Under Buttocks (UB) Drape • The Hysteroscope Outflow Channel • Optional: The MyoSure Tissue Removal Device (TRD). Use only if performing MyoSure procedure.
System Setup Perform the System Setup steps in the order that is most logical for your facility. Handle all materials according to your facility’s protocol. Perform the following steps to prepare the Fluent Fluid Management System for use. Hang the Fluid Bag
WARNING! The maximum amount of weight should not exceed 6L of fluid. Doing so may negatively impact fluid deficit accuracy. 1. Hang up to 6L of fluid from the IV Pole with distension media appropriate for the procedure. If you need to replace a Fluid Bag during the procedure, see the Chapter 6: Replacing Components.
Note: The Fluent Fluid Management System does not need to be powered on to hang the Fluid Bags. If it is on, then follow the prompts. After the Fluid Bags have been hung properly, the system displays a green check mark. Waste Bag Hanger
Unpack the Fluent Procedure Kit 2a. Open the Fluent Procedure Kit package. 2b. Set the non-sterile Waste Bag aside. 2c. Peel back the sterile seal to open the Fluent In-FloPak and Fluent Out-FloPak and place them on a sterile surface. Hang the Waste Bag
WARNING! The maximum amount of weight should not exceed one full Waste Bag (6kg). This can negatively impact fluid deficit accuracy. 3. Hang a new Waste Bag on the Waste Bag Hanger to begin any new procedure. After the Waste Bag has been hung properly, the system displays a green check mark.
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Chapter 3: Connecting the System Components
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