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Armstrong Medical AquaVENT FD140 Instructions For Use Manual

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CRITICAL CARE
AquaVENT
FD140
®
Instructions for use

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  • Page 1 CRITICAL CARE AquaVENT FD140 ® Instructions for use...
  • Page 2 The device operates as described in these instructions for use, enclosed documents and on equipment labelling, provided that it is assembled, operated, maintained and repaired according to the enclosed documentation. The device must be inspected at regular intervals. The device must not be used if found to be defective. Damaged, missing, clearly worn out, warped or contaminated parts must be replaced immediately.

  • Page 3: Table Of Contents

    Contents 0 Contents 1 Introduction 1.1 About this manual 1.2 Symbols used in the instructions for use and on the device 1.3 Abbreviations used in the instructions for use and on the device 2 Safety 2.1 Safety precautions 3 General description 3.1 Intended use 3.2 Main components 3.3 Operation...
  • Page 4 0 Contents 5 Operation 5.1 Switching power on and off 5.2 System test 5.3 Mode selection 5.4 Standby 5.5 Parameter adjustment 5.5.1 Changing patient airway pressure during therapy 5.5.2 Treatment duration 5.5.3 FiO 5.5.4 Flow adjustment 5.6 Patient menu 5.6.1 Alarm volume 5.6.2 Apnoea alarm 5.6.3 P max 5.6.4 P min...
  • Page 5 0 Contents 9.6 Measuring functions 9.7 Paramagnetic oxygen sensor 9.8 Display 9.9 Alarms 9.10 External communication 9.11 Guidance and manufacturer's declaration 10 Navigation & accessories 10.1 Navigation 10.2 Accessories ® Instructions for Use, AquaVENT FD140, Rev. 12...
  • Page 6 0 Contents - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 7: Introduction

    Introduction In this chapter 1.1 About this manual 1.2 Symbols used in the instructions for use and on the device 1.3 Abbreviations used in the instructions for use and on the device ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 8: About This Manual

    1 Introduction 1.1 About this manual These instructions for use describe the intended use of the following product: ® AquaVENT FD140 with software version 1.13.0 and hardware version 1.02 For a list of the approved accessories, please refer to chapter 10.2 Accessories.

  • Page 9: Symbols Used In The Instructions For Use And On The Device

    1 Introduction 1.2 Symbols used in the instructions for use and on the device Refers to dangerous situations which may occur when failing to observe the present instructions for use. Refers to a situation which may cause injuries to the user or Warning the patient.

  • Page 10: Abbreviations Used In The Instructions For Use And On The Device

    1 Introduction Power indicator Three-level capacity indicator of the rechargeable battery ON/OFF key Serial interface AquaVENT® FD140 corresponds Directive 93/42/EEC concerning medical devices, provided it is operated according to the instructions for use. "0123" is the identification number of the notified body. Follow the instructions for use.

  • Page 11: Safety

    Safety In this chapter 2.1 Safety precautions ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 12: Safety Precautions

    2 Safety 2.1 Safety precautions Reference: These instructions for use describe the product: ® AquaVENT FD140 CPAP respiratory therapy device Software version 1.13.0 Hardware version 1.02 Safe operation: ® In order to guarantee the safe operation of the AquaVENT FD140, the ®...
  • Page 13 2 Safety Safety functions: ® The following safety functions were implemented in the AquaVENT FD140 in order to warn the user if the patient is at risk: Device alarms: Monitoring Monitoring for of AIR gas supply, loss of AIR supply, of O gas supply loss of O...
  • Page 14 2 Safety Electrical hazard: ® The AquaVENT FD140 is exclusively designed for use in an electrical environment according to VDE 0100 part 710 or EN 60601-1. ® The AquaVENT FD140 must not be used if there are doubts concerning the quality and function of the protective earthing of the electrical installation.
  • Page 15 2 Safety The use of other electrical devices, e.g., power cords, may result in increased emissions or decreased Warning ® immunity performance of the AquaVENT FD140. This may put the patient at risk. ® Using other electrical devices with the AquaVENT FD140 or in its vicinity can cause interference.
  • Page 16 2 Safety - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 17: General Description

    General description In this chapter 3.1 Intended use 3.2 Main components 3.3 Operation 3.4 Operating principle 3.4.1 CPAP mode 3.4.2 High Flow Oxygen Therapy (HFOT) mode 3.4.3 Helmet CPAP mode 3.4.4 Paed CPAP mode ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 18: Intended Use

    3 General description 3.1 Intended use ® The AquaVENT FD140 is a clinical respiratory therapy device which assists respiration with constant positive air pressure (CPAP and HFOT), and can be used for administering aerosol medication. The connected patient (without direct supervision by staff or monitoring equipment) must be ®...

  • Page 19: Main Components

    3 General description 3.2 Main components Front: Alarm pause Touch screen Menu key Pressure measuring line Power connection indicator ON/OFF key Respiratory Nebuliser gas outlet port ® Instructions for Use, AquaVENT FD140, Rev. 12...
  • Page 20 3 General description Back: Serial interface Power input inlet AIR inlet Type plate Display: Patient airway pressure (bar graph) Nebuliser Patient airway pressure (set value) Battery capacity indication Treatment duration Respiratory rate Flow indication ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 21: Operation

    3 General description 3.3 Operation ® The AquaVENT FD140 has a touch screen, which allows parameters and alarm thresholds to be set by pressing the relevant field on the touch screen as well as to pause or confirm alarms. Further operating controls are the ON/OFF key, the Menu key and the Alarm pause key.

  • Page 22: Paed Cpap Mode

    3 General description 3.4.4 Paed CPAP mode The flow provided at the respiratory gas outlet is constant and user- adjustable. The maximum flow in this mode is 70 l/min. ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 23: Preparing The Device For Operation

    Preparing the device for operation In this chapter 4.1 General information 4.2 Power supply 4.2.1 Mains supply 4.2.2 Rechargeable battery 4.3 Gas supply 4.3.1 Two-gas operation 4.3.2 Single-gas operation 4.4 CPAP breathing circuit 4.5 CPAP with face mask, unheated 4.6 CPAP with face mask, heated 4.7 Nebulised drug delivery 4.8 High Flow Oxygen Therapy (HFOT) mode 4.9 Helmet CPAP application...

  • Page 24: General Information

    4 Preparing the device for operation 4.1 General information Before each use, the device must be checked for visible damage. Caution ® A quick reference guide for putting the AquaVENT FD140 into operation is provided in chapter 10 Navigation. 4.2 Power supply 4.2.1 Mains supply ®...

  • Page 25: Rechargeable Battery

    4 Preparing the device for operation Connect the original power cord to the power input on the back of the device. The power cord is protected against accidental disconnection. This retainer closes automatically when the cord is plugged into the power input. To remove the power cord, first press on the red lock of the power cord and then, holding the lock depressed, remove the plug.
  • Page 26 4 Preparing the device for operation charged, the minute value of the operating time is not shown. ® When the AquaVENT FD140 is connected to the mains and the power indicator illuminates green, the internal battery charges automatically. Note The internal battery used is a lead-acid battery. A fully charged battery can be stored for up to 3 months, after which it requires charging.

  • Page 27: Gas Supply

    4 Preparing the device for operation 4.3 Gas supply 4.3.1 Two-gas operation ® The AquaVENT FD140 is equipped with an electronic gas mixer for oxygen ) and air (AIR). The mixer must be supplied with both gases at a supply pressure ranging from 270 to 600 kPa.

  • Page 28: Single-Gas Operation

    4 Preparing the device for operation Ensure that only dry and clean gases are used. Water, oil or particles entering the device can damage the device Warning and endanger the patient. 4.3.2 Single-gas operation ® The design of the AquaVENT FD140 allows it to be operated with a single gas supply at any time.

  • Page 29: Cpap Or Paed Cpap With Face Mask, Unheated

    4 Preparing the device for operation 4.5 CPAP or Paed CPAP with face mask, unheated Connect the breathing circuit as shown in the following diagram: ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 30: Cpap Or Paed Cpap With Face Mask, Heated

    4 Preparing the device for operation 4.6 CPAP or Paed CPAP with face mask, heated An active humidifier must be integrated in the heated CPAP breathing circuit. Note To prevent water from the humidifier, which collects during ® operation, from entering the AquaVENT FD140, the active humidifier should be placed at a level below that of the ®...
  • Page 31 4 Preparing the device for operation Assemble the breathing circuit as shown in the following diagram: ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 32: Nebulised Drug Delivery

    4 Preparing the device for operation 4.7 Nebulised drug delivery When the jet nebuliser function is used, the patient receives medical aerosol via the CPAP breathing circuit during the therapy. The approved nebulisers are specified in chapter 10.2 Accessories. Please refer to chapter 1.1 About this manual for details.
  • Page 33 4 Preparing the device for operation The nasal cannula is connected to the breathing circuit in close proximity to the patient. The breathing circuit is basically identical with the illustration in chapter 4.6. Be sure to adjust the required flow according to the instructions provided by the manufacturer of the nasal Warning cannula to avoid accidental pressure peaks.

  • Page 34: Helmet Cpap Application

    4 Preparing the device for operation 4.9 Helmet CPAP application ® The AquaVENT FD140 supports non-invasive ventilation by means of a CPAP helmet. Connect the CPAP helmet to the AquaVent FD140 as shown below: ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 35: Placement Of The Device

    4 Preparing the device for operation Note Observe all instructions provided by the manufacturer of the accessories. Be sure to adjust the required flow according to the instructions provided by the manufacturer of the CPAP Warning helmet to avoid accidental CO rebreathing.
  • Page 36 4 Preparing the device for operation - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 37: Operation

    5 Operation Operation In this chapter 5.1 Switching power on and off 5.2 System test 5.3 Mode selection 5.4 Standby 5.5 Parameter adjustment 5.5.1 Changing patient airway pressure during therapy 5.5.2 Treatment duration 5.5.3 FiO 5.5.4 Flow adjustment 5.6 Patient menu 5.6.1 Alarm volume 5.6.2 Apnoea alarm 5.6.3 P max...

  • Page 38: Switching Power On And Off

    5 Operation 5.1 Switching power on and off Switching power on: ® When the AquaVENT FD140 is connected to an AC power supply (see chapter 4.2 Power supply), the LED above the power symbol is green. Now, ® the AquaVENT FD140 can be switched on with the ON/OFF key at the bottom right.
  • Page 39 5 Operation Switching power off: ® The AquaVENT FD140 can be switched off as follows: Press the ON/OFF key and confirm the command by touching 'Yes'. When you select 'No', you return to the previous screen. ® The AquaVENT FD140cannot be switched off while in the therapy mode. Terminate the therapy mode first by pressing the ON/OFF key and by entering the standby mode.

  • Page 40: System Test

    5 Operation 5.2 System test The system test starts automatically after power-on and takes about 5 seconds. During this period, the background colour changes from red to yellow and eventually to green. In addition, the device emits two consecutive audio signals: the first signal at a volume level of 50%, the second signal at the last selected volume level.

  • Page 41: Mode Selection

    5 Operation During the system test, all pneumatic components, their electronic control, and further safety-related components are tested. If the system test reveals a malfunction, a corresponding message is shown on the screen. Please refer to chapter 6 Alarms and messages for error message details. After a successful system test, the mode menu will be displayed.
  • Page 42 5 Operation The display background colours are green for the helmet CPAP mode, white for the Paed CPAP mode, blue for the HFOT mode and purple for the CPAP mode. After selection of a mode, the screen display changes and you can adjust the flow: Touch the vertical line under the numerical value (flow in l/min) and drag it along the horizontal line until you reach the desired flow value.

  • Page 43: Standby

    5 Operation 5.4 Standby In the standby mode, different device settings can be configured before starting the therapy. Fields where adjustments can be carried out are displayed with a border. A field is activated by touching it. 1: Start The therapy screen is displayed and patient treatment starts. Please refer to chapter 5.7 Starting/ending therapy for details.

  • Page 44: Parameter Adjustment

    5 Operation 5.5 Parameter adjustment 5.5.1 Changing patient airway pressure during therapy In the CPAP and helmet CPAP modes, the patient airway pressure can be adjusted by changing the PEEP valve during the treatment. In the CPAP and helmet CPAP modes, the patient airway pressure field shows the measured patient airway pressure, which is averaged over a longer period of time.

  • Page 45: Treatment Duration

    5 Operation 5.5.2 Treatment duration The measurement of the treatment duration in minutes and seconds can be started during the therapy by pressing the appropriate field on the touch screen. The stopwatch (0:00) changes its colour briefly to indicate that it has been activated.

  • Page 46: Fio 2

    5 Operation In the standby mode, the user can only reset the timer. Pressing the dimmed field resets the timer to 0:00. The maximum treatment duration which can be measured is 99 minutes and 59 seconds. When the maximum value is reached, the stopwatch instantly rolls over to 0 minutes and 0 seconds.

  • Page 47: Flow Adjustment

    5 Operation Note In the first 60 seconds after a change of the flow value in the therapy mode, all patient alarms and FiO alarms are deactivated. Please refer to chapter 6.1 Alarms for details. ® Note With patients dependent on a higher, defined FiO , AquaVENT FD140 with integrated paramagnetic oxygen sensor must be used.
  • Page 48 5 Operation A window for adjustment of the continuous flow opens: Touch the vertical line under the value (flow in l/min) and drag it along the horizontal line until you reach the desired flow value. Alternatively, you can touch the screen directly below the desired value. Press 'OK' to confirm the setting.

  • Page 49: Patient Menu

    5 Operation A setting can be selected only when the user returns to the permitted range and the 'OK' button is displayed again. Note In the first 60 seconds after a change of the flow value in the therapy mode, all patient alarms and FiO alarms are deactivated.

  • Page 50: Apnoea Alarm

    5 Operation 5.6.2 Apnoea alarm A menu is provided for setting the apnoea alarm. Press the menu key in the standby mode or therapy mode to display the menu. Press 'Apnoea' to enter the setting mode. The label appears in reverse video now, which means that the apnoea parameter can be adjusted.

  • Page 51: P Min

    5 Operation Press the Menu key to save the selected pressure limit. The standby or therapy screen is displayed again. 5.6.4 P min A menu is provided for setting the minimum airway pressure. To access the menu, press the Menu key in the standby or therapy mode, then select 'page 2'.

  • Page 52: Starting/Ending Therapy

    5 Operation Press 'F max' to enter the setting mode. The label appears in reverse video now, which means that the F max parameter can be adjusted. Set the desired limit value by pressing the + and - fields. You can turn off the F max value or set a rate in the range from 1 to 60 breaths per minute as the alarm limit.

  • Page 53: Activating/Deactivating The Nebuliser

    5 Operation Patient airway pressure (bar graph) Nebuliser Patient airway pressure (set value) Battery capacity indication Treatment duration Flow indication Respiratory rate Press the ON/OFF key to terminate or suspend the therapy. You will then see a standby field in the therapy screen. ON/OFF ®...
  • Page 54 5 Operation Note The nebuliser is completely deactivated in the helmet CPAP mode and cannot be used. The nebuliser is operated with compressed air. During the treatment, the compressed air is added to the mixture in the breathing circuit. Therefore, the nebuliser function is only available up to specific O concentrations to allow patients dependent on a higher, defined FiO...
  • Page 55 5 Operation In the CPAP mode or Paed CPAP mode, the user defines a constant gas flow. If the gas flow, in conjunction with a desired oxygen concentration is insufficient for use of the nebuliser, the device will specify a minimum flow and displays an appropriate message.
  • Page 56 5 Operation - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 57: Alarms And Messages

    Alarms and messages In this chapter 6.1 Alarms 6.2 Messages 6.2.1 Messages during the system test 6.2.2 Messages during the CPAP test ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 58: Alarms

    6 Alarms and messages 6.1 Alarms The alarm management system differentiates between different priorities: Notice green background no audible signal Low priority yellow background single audible signal three consecutive beeps at 15- Medium priority red background second intervals and with increasing volume The alarm message is displayed in the lower part of the screen.
  • Page 59 6 Alarms and messages Corrective Message Trigger condition Info measure patient pressure patient pressure > < 25 cmH 25 cmH O or > no alarm delay, gas P limit or < CPAP CPAP + 10 cmH flow reduced (1 l/min) + 10 cmH (whichever is higher) (whichever is...
  • Page 60 6 Alarms and messages Message Trigger condition Corrective measure no measured values from contact authorised service Sensor defect pressure sensors technician key or touch screen Key/ Touch? pressed for more than release key or touch screen 5 seconds Battery still connect to mains power and battery capacity <...

  • Page 61: Messages

    6 Alarms and messages Message Trigger condition Corrective measure measured FiO is at least measured FiO is not at least FiO2 high 5% higher than the set 5% higher than the set value value measured FiO is at least measured FiO is not at least 5% below the set value or FiO2 low...

  • Page 62: Messages During The System Test

    6 Alarms and messages signal. Error messages (medium priority) are displayed on a red background; they are numbered and accompanied by an audio signal. 6.2.1 Messages during the system test Messages occurring during the system test are represented as follows: As soon as the trigger condition for the message no longer exists, the CPAP screen will be displayed.
  • Page 63 6 Alarms and messages Corrective Message Trigger condition Info measure No line connect device voltage. to mains or check mains Continue no connection to mains confirm connection with battery operation on supply? battery power Battery confirm defect battery not ready for continued Continue operation...

  • Page 64: Messages During The Cpap Test

    6 Alarms and messages Corrective Message Trigger condition Info measure Connect O and/or No O2 or No O or AIR at gas AIR to AIR supply inlets appropriate gas inlet contact Fan defect do not use the authorised slow fan speed Call service device service...
  • Page 65 6 Alarms and messages Corrective Message Trigger condition Info measure press 'Return' CPAP test was CPAP lower than and set CPAP restart started with CPAP 3.0 cmH2O value CPAP test value < 3 cmH2O > 3 cmH2O CPAP test was started press 'Return' No gas restart...
  • Page 66 6 Alarms and messages - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 67: Cleaning

    Cleaning In this chapter 7.1 General information 7.2 Cleaning and disinfection ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 68: General Information

    7 Cleaning 7.1 General information Important safety precautions: Warning  Read the instructions for use and the data sheets of the cleaning agents to be used.  Wear protective gloves and safety goggles.  Do not inhale fumes. Avoid damages: Caution ...

  • Page 69: Cleaning And Disinfection

    7 Cleaning 7.2 Cleaning and disinfection Housing: ® Switch off the AquaVENT FD140 and check that the mains plug was removed. Use a soft cloth and mild detergents to clean the surface of the housing. ® "mikrozid sensitive liquid" by "Schülke & Mayr GmbH" (www.schuelke.com) is recommended for disinfection of the surface (use per manufacturer's instructions).
  • Page 70 7 Cleaning - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 71: Maintenance

    Maintenance In this chapter 8.1 General information 8.1.1 Annual maintenance 8.1.2 Maintenance every two years 8.1.3 Maintenance every six years 8.1.4 Maintenance every 12 years 8.2 O sensor calibration ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 72: General Information

    8 Maintenance 8.1 General information ® The AquaVENT FD140 has been designed as a CPAP therapy device that requires minimal maintenance. Maintenance must be performed annually by an authorised service technician. Note For detailed information about maintenance, please refer to the Technical Manual. All servicing must be carried out by authorised service Warning technicians only.

  • Page 73: Maintenance Every Six Years

    8 Maintenance 8.1.3 Maintenance every six years Every six years, the maintenance includes:  the replacement of the O pressure regulator 8.1.4 Maintenance every 12 years ® It is necessary to replace all active internal components of the AquaVENT FD140 for safety reasons during maintenance after 12 years. ®...

  • Page 74: O 2 Sensor Calibration

    8 Maintenance 8.2 O sensor calibration In some instances, i.g. after vibrations caused by transport, the O sensor might need to be recalibrated. The following alarm message will appear. Press “Yes” to start the calibration process. You may also want to calibrate the O -Sensor if the values are out of the tolerances.
  • Page 75 8 Maintenance Remark To avoid influence of ambient air on the O sensor, connect a tube to the inspiration port. Remark The calibration routine requires AIR and O gas supply. If the supply of at least one gas is missing or breaks down during calibration, a message will appear: ‘Connect O2 and AIR’...
  • Page 76 8 Maintenance - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 77: Technical Specifications

    In this chapter 9.1 General information 9.2 Supply 9.2.1 Power supply 9.2.2 Gas supply 9.3 Technical specifications of the AquaVent FD140 9.4 Increments and intervals of parameter settings 9.5 Default settings 9.6 Measuring functions 9.7 Paramagnetic oxygen sensor 9.8 Display 9.9 Alarms...

  • Page 78: General Information

    9 Technical specifications 9.1 General information Application: Intended use: see chapter 3.1 Intended use Area: general therapy Use: hospital Patient categories: adults children greater than 5 kg in weight Dimensions and weight: Width x depth x height: 260 x 244 x 210 mm Minimum footprint: 270 cm²...

  • Page 79: Supply

    9 Technical specifications Classification: Device class according to Directive 93/42/EEC, Annex IX: Protection class, electrical hazard: I (protective earth) Mode of operation (duration of application) short-term application Languages: German, English, French, Italian, Dutch (contact an authorised service technician if you want to select another language) 9.2 Supply 9.2.1 Power supply...

  • Page 80: Technical Specifications Of The Aquavent Fd140

    9 Technical specifications ® 9.3 Technical specifications of the AquaVENT FD140 Therapy: CPAP: Therapy mode: depending on PEEP valve used flow adjustment range: 20 to 140 l/min Paed CPAP: depending on PEEP valve used flow adjustment range: 10 to 70 l/min HFOT: flow adjustment range: 0 to 60 l/min Helmet CPAP:...

  • Page 81: Measuring Functions

    9 Technical specifications Apnoea 20 s P max 12 cm H P min 2 cm H F max 9.6 Measuring functions Increment Min. Max. value Accuracy value Flow 1 l/min 0 l/min 200 l/min ± 10% Respiratory 1 /min 0 /min 60 /min ±...

  • Page 82: External Communication

    9 Technical specifications 9.10 External communication ® For communication with external devices, the AquaVENT FD140 has an RS232 interface for output of status and measurement data as well as settings. Please contact the manufacturer for the exact specifications. The contact details are stated on the back cover.
  • Page 83 9 Technical specifications Electromagnetic immunity: ® The AquaVENT FD140 is intended for use in the electromagnetic environment specified below. It is the responsibility of the user and/or ® operator of the AquaVENT FD140 to ensure that the device is operated in such an environment.
  • Page 84 9 Technical specifications IEC 60601 test Compliance Electromagnetic Immunity test level level environment - guidance The mains power quality < 5% U (> 95% < 5% U (> 95% should be that of a typical dip in der U ) for dip in der U ) for commercial or hospital...
  • Page 85 9 Technical specifications Immunity IEC 60601-1-2 Compliance Electromagnetic environment - test test level level guidance Portable and mobile RF communications equipment should be used no closer to the ® AquaVENT FD140, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Conducted ...
  • Page 86 9 Technical specifications Note 1 At 80 MHz and 800 MHz, the higher frequency range applies. Note 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
  • Page 87 9 Technical specifications Recommended separation distances between portable and mobile RF ® communications equipment and the AquaVENT FD140 ® The AquaVENT FD140 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the ®...
  • Page 88 9 Technical specifications - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev.12...

  • Page 89: Navigation & Accessories

    Navigation & accessories In this chapter 10.1 Navigation 10.2 Accessories ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 90: Navigation

    9 Technical specifications 10.1 Navigation CPAP mode Press ON/OFF key to switch the AquaVent Mode selection System test starts automatically Patient airway pressure field Start CPAP therapy Stopwatch for treatment duration ® Instructions for Use, AquaVENT FD140, Rev.12...
  • Page 91 10 Navigation Paed CPAP mode Press ON/OFF key to switch the AquaVent Mode selection System test starts automatically Patient airway pressure field Start Paed CPAP therapy Stopwatch for treatment duration...
  • Page 92 9 Technical specifications High Flow Oxygen Therapy (HFOT) mode Press ON/OFF key to switch the AquaVent Mode selection System test starts automatically Patient airway pressure field Start helmet CPAP therapy Stopwatch for treatment duration ® Instructions for Use, AquaVENT FD140, Rev.12...
  • Page 93 Helmet CPAP mode Press ON/OFF key to switch the AquaVent Mode selection System test starts automatically Patient airway pressure field Start helmet CPAP therapy Stopwatch for treatment duration ® Instructions for Use, AquaVENT FD140, Rev. 12...

  • Page 94: Accessories

    10.2 Accessories Code Description AMPV9003 CLARITI CPAP PEEP valve, 2.5cmH AMPV9005 CLARITI CPAP PEEP valve, 5cmH AMPV9007 CLARITI CPAP PEEP valve, 7.5cmH AMPV9010 CLARITI CPAP PEEP valve, 10cmH AMPV9012 CLARITI CPAP PEEP valve, 12cmH AMPV9015 CLARITI CPAP safety valve, 15cmH AMPV9020 CLARITI CPAP safety valve, 20cmH T-piece for tracheal connection,...
  • Page 95 - This page is intentionally blank. - ® Instructions for Use, AquaVENT FD140, Rev. 12...
  • Page 96 Manufacturer of the Salvia medical GmbH & Co. KG ® AquaVENT FD140 Niederhöchstädter Str. 62 61476 Kronberg Germany Telephone: +49 (0) 6173 9333-0 Fax: +49 (0) 6173 9333-29 info@salvia-medical.de www.salvia-medical.de ® Instructions for Use, AquaVENT FD140 Part number: CM-929450 Revision: 12 Date: 02.02.2016 Subject to modifications.

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