368493r1 S9 VPAP ST-A Information Guide AMER Eng Ref
Contents
1. Flow derived values Leak 0 200 L min 1 L min Tidal volume 0 4000 mL 1 mL Respiratory rate 0 50 BPM 1 BPM Minute ventilation 0 30 L min 0 1 L min Ti 0 1 4 0 sec 0 1 sec I E ratio 1 50 2 71 0 1 Value Accuracy Pressure measurement Mask pressure 0 5 cm H20 4 of measured value Flow measurements Leak 12 L min or 20 of reading whichever is greater at O to 60 L min Tidal volume 20 Respiratory rate gt 1 BPM Minute ventilation 20 a Results are expressed at ATPD Ambient Temperature and Pressure Dry b Accuracy may be reduced by the presence of leaks supplemental oxygen tidal volumes lt 100 mL or minute ventilation lt 3 L min c Measurement accuracy verified as per EN ISO 10651 6 2009 for Home Care Ventilatory Support Devices Figure 101 and Table 101 Pressure accuracy Maximum static pressure variation at 10 cm H20 according to EN ISO 17510 1 2009 Without H5i With H5i Standard air tubing 9 89 cm H20 to 9 97 cm H20 9 82 cm H20 to 9 98 cm H20 SlimLine air tubing 9 76 cm H20 to 9 87 cm H20 9 78 cm H20 to 9 88 cm H20 Maximum dynamic pressure variation according to EN ISO 17510 1 2009 Pressure cm H20 4 8 12 16 20 25 Pressure cm H20 12 16 20 25 10 BPM 15 BPM 20 BPM VPAP ST A and Standard air tubing without H5i VPAP ST A and Standard 0 18 0 18 0 21 0 20 0 21 0 20 0 22 0 21 0 23 0 22 0 30 0 31 10 BPM air tubing with H5i 0 302. and humidifier if used Problem Possible cause Solution Alarm is activated and the LCD screen display disappears Power failure Remove your mask until power is restored Power cord is disconnected or Ensure the power cord is connected and the mains power switch mains power switch is turned if available is on off during therapy English 5 Problem Possible cause Solution Displays message High leak please check system setup and all connections There is excessive leak Adjust position of mask and headgear Connect the air tubing firmly at both ends Displays message No tube please check your tube is connected Flow is high because air tubing Connect the air tubing firmly at both ends is not connected properly Note The tube disconnection check may not operate when an antibacterial filter is used Displays message Tube blocked please check your tube Air tubing is blocked Check your air tubing and remove any blockages Disconnect the power cord and then reconnect it to restart the device Displays message No SpO2 data check oxi sensor attachment to module finger Oximeter sensor is not attached Ensure that the oximeter sensor is attached properly to the module properly and the patient s finger Oximeter sensor might be If the message appears repeatedly but the oximeter is attached faulty properly to the module and the patient s finger the oximeter sensor might be faulty Contact your service provider or ex
3. 0 30 0 26 0 24 0 26 0 23 0 27 0 26 0 26 0 28 0 54 0 50 15 BPM 0 51 0 5 0 38 0 36 0 34 0 3 0 36 0 33 0 38 0 35 0 74 0 7 20 BPM VPAP ST A and SlimLine air tubing without H5i VPAP ST A and SlimLine 0 22 0 20 0 23 0 19 0 22 0 21 0 22 0 23 0 24 0 27 0 31 0 31 air tubing with H5i 0 28 0 29 0 32 0 29 0 35 0 29 0 41 0 33 0 37 0 34 0 50 0 54 0 47 0 53 0 41 0 42 0 41 0 45 0 44 0 50 0 48 0 50 0 78 0 84 English 13 Symbols The following symbols may appear on your product or packaging A Caution Read instructions before use IP21 Protection against insertion of fingers and against A oe vertically dripping water Al type BF equipment Class II equipment O Start Stop ual Manufacturer ECIREP European Authorised Representative Ke European RoHS LOT Batch code REF Catalogue number LSN_ Serial number Direct current e Y Lock unlock China pollution control logo 1 020 China pollution control logo 2 IP20 Not drip proof a Keep dry Alarm mute key Environmental information WEEE 2002 96 EC is a European Directive that requires the proper disposal of electrical and electronic equipment This device should be disposed of separately not as unsorted municipal waste To dispose of your device you should use appropriate collection reuse and recycling systems available in your region The use of these colle
4. Explosion hazard do not use in the vicinity of flammable anesthetics e Make sure the power cord and plug are in good condition and the equipment is not damaged Keep the power cord away from hot surfaces e The device should only be used with masks and connectors recommended by ResMed or by a physician or respiratory therapist A mask should not be used unless the device is turned on Once the mask is fitted ensure that the device is blowing air The vent hole or holes associated with the mask should never be blocked 1 Ports may be incorporated into the mask or in connectors that are near the mask 16 Explanation The device is intended to be used with special masks or connectors which have vent holes to allow continuous flow of air out of the mask When the device is turned on and functioning properly new air from the device flushes the exhaled air out through the mask vent holes However when the device is not operating insufficient fresh air will be provided through the mask and the exhaled air may be rebreathed Rebreathing of exhaled air for longer than several minutes can in some circumstances lead to suffocation This applies to most models of CPAP or bilevel devices Oxygen supports combustion Oxygen must not be used while smoking or in the presence of an open flame Always ensure that the device is turned on and airflow generated before the oxygen supply is turned on Always turn the oxygen supply off before the de
5. ResMeEpD VPAP ST A iVAPS VPAP ST A NONINVASIVE VENTILATOR Information Guide English Please read the entire Information and Welcome Guides before using the VPAP ST A or VPAP ST A iVAPS hereafter VPAP ST A Note The iVAPS mode is not available in all devices Asia Pacific VPAP ST A indications for use The VPAP ST A is indicated to provide noninvasive ventilation for patients weighing more than 13 kg or more than 30 kg in iVAPS mode with respiratory insufficiency or obstructive sleep apnoea OSA The VPAP ST A is intended for home and hospital use The Nordic countries and the UK VPAP ST A iVAPS indications for use The VPAP ST A iVAPS is indicated to provide noninvasive ventilation for patients weighing more than 13 kg or more than 30 kg in iVAPS mode with respiratory insufficiency or obstructive sleep apnoea OSA The VPAP ST A iVAPS is intended for home and hospital use VPAP ST A indications for use The VPAP ST A is indicated to provide noninvasive ventilation for patients weighing more than 13 kg with respiratory insufficiency or obstructive sleep apnoea OSA The VPAP ST A is intended for home and hospital use Contraindications Positive airway pressure therapy may be contraindicated in some patients with the following pre existing conditions severe bullous lung disease pneumothorax or pneumomediastinum pathologically low blood pressure particularly if associated with intrava
6. arding the electromagnetic emissions and immunity of this ResMed device can be found on www resmed com on the Products page under Service and Support Click on the PDF file for your language Class II double insulation Type BF Ingress protection IP21 VPAP ST A technical specifications Mode pressure ranges Maximum single fault pressure Physical Air filter Sound DECLARED DUAL NUMBER NOISE EMISSION VALUES in accordance with ISO 4871 1996 Alarm volume settings CPAP mode Set Pressure 4 20 cm H20 S ST T and PAC modes PAP 4 30 cm H20 EPAP 2 25 cm H20 iVAPS mode PS 0 28 cm H20 EPAP 2 25 cm H20 aximum single fault steady state pressure 30 cm H2O if pressure exceeded for gt 6 sec 40 cm H2O if pressure exceeded for gt 1 sec ominal dimensions L x W x H 153 mm x 172 mm x 86 mm Weight 1 04 kg Housing construction Flame retardant engineering thermoplastic Air outlet 22 mm conical air outlet complies with ISO 5356 1 2004 Hypoallergenic air filter Acrylic and polypropylene fibers in a polypropylene carrier Standard air filter Polyester non woven fiber Pressure level CPAP mode With SlimLine air 26 dBA with uncertainty of 2 dBA as measured according ubing to EN ISO 17510 1 2009 With Standard air 27 dBA with uncertainty of 2 dBA as measured according ubing to EN ISO 17510 1 2009 With either SlimLine 28 dBA with uncertainty of 2 dBA as measured acco
7. change the oximeter Displays message Non vented mask use vented mask or unblock mask vents Non vented mask is used Only use a vented mask Mask vents might be blocked Check if you have sufficient venting Unblock mask vents if necessary A low EPAP in conjunction with Talk to your clinician about your settings supplemental oxygen may result in false triggering of this alarm on a vented mask Problem Possible cause Solution Displays message No oximeter check connect oximeter adapter Oximeter adapter is not Ensure that the oximeter adapter is attached properly attached properly Oximeter adapter might be If the message appears repeatedly but the oximeter adapter is faulty attached properly the oximeter adapter might be faulty Contact your service provider Displays message Check ResMed 30 90W Power Supply Unit The power supply unit is being Make sure that the power supply unit is free from bedding clothes covered by bedding or other objects that could cover it The power supply unit is Let the power supply unit cool down overheated The DC plug is partially inserted Fully insert the DC plug into the back of the device or inserted too slowly Displays message Alarm module fault please contact service provider General failure of the device Contact your service provider immediately and or the alarm module Therapy cannot be started again English 7 General technical specifications Power supply En
8. ction reuse and recycling systems is designed to reduce pressure on natural resources and prevent hazardous substances from damaging the environment If you need information on these disposal systems please contact your local waste administration The crossed bin symbol invites you to use these disposal systems If you require information on collection and disposal of your ResMed device please contact your ResMed office local distributor or go to www resmed com environment Servicing The VPAP ST A device is intended to provide safe and reliable operation when operated in accordance with the instructions provided by ResMed ResMed recommends that the VPAP ST A device be inspected and serviced by an authorised ResMed Service Centre if there is any sign of wear or concern with device function Otherwise service and inspection of the devices generally should not be required during the five year design life of the device Limited warranty ResMed Ltd hereafter ResMed warrants that your ResMed product shall be free from defects in material and workmanship from the date of purchase for the period specified below Product Warranty period Mask systems including mask frame cushion headgear and 90 days tubing excluding single use devices Accessories excluding single use devices Flex type finger pulse sensors Humidifier water tubs e Batteries for use in ResMed internal and external battery 6 months systems e Clip type fing
9. e cause Solution Incorrect air tubing selected If you are using the SlimLine Standard or 3 m air tubing ensure that you have the correct air tubing selected via the menu Non vented mask is used Only use a vented mask Mask vents might be blocked Check if you have sufficient venting Unblock mask vents if necessary EPAP may be set too low Talk to your clinician about your settings Device does not start when you breathe into the mask Breath is not deep enough to Take a deep breath in and out through the mask trigger SmartStart Stop SmartStart Stop is disabled Press Start Stop to start therapy because the High Leak or Low Minute Ventilation alarm is enabled SmartStart Stop is disabled Talk to your clinician about enabling the SmartStart Stop feature There is excessive leak Adjust position of mask and headgear Connect the air tubing firmly at both ends Device does not stop when you remove your mask SmartStart Stop is disabled Press Start Stop to stop therapy because the High Leak or Low Minute Ventilation alarm is enabled SmartStart Stop is disabled A message appears on the screen To stop therapy select Yes and because Confirm Stop is press the Push Dial enabled SmartStart Stop is disabled Talk to your clinician about enabling the SmartStart Stop feature SmartStart Stop is enabled but the device does not stop automatically when you remove your mask Incompatible mask system Only use equipment r
10. ecommended by ResMed being used English 3 Problem Possible cause Incorrect mask setting being used The patient is using a nasal pillows mask with a set pressure less than 6 cm H20 The patient is using a paediatric mask with a set pressure less than 8 cm H20 Pressure rises inappropriately Talking coughing or breathing in an unusual manner Mask cushion is buzzing against the skin Cushion seated incorrectly causing excessive leak Solution Check the selected mask type in the Setup menu Change it if necessary Disable SmartStart Stop Disable SmartStart Stop Avoid talking with a nasal mask on and breathe as normally as possible Adjust the headgear Adjust headgear or re fit cushion Displays message High temperature fault refer to user manual Device has been left in a hot environment Air filter is blocked Air tubing is blocked Humidity level setting is too high resulting in accumulation of water in the air tubing Allow to cool before re use Disconnect the power cord and then reconnect it to restart the device Replace your air filter Disconnect the power cord and then reconnect it to restart the device Check your air tubing and remove any blockages Disconnect the power cord and then reconnect it to restart the device Turn the humidity level setting down and empty the water from the air tubing Displays message Check ResMed 30 90W Power Supply Unit and fully insert the c
11. er pulse sensors 1 year CPAP and bilevel device data modules Oximeters and CPAP and bilevel device oximeter adapters Humidifiers and humidifier cleanable water tubs Titration control devices CPAP bilevel and ventilation devices including external 2 years power supply units e Battery accessories e Portable diagnostic screening devices This warranty is only available to the initial consumer It is not transferable If the product fails under conditions of normal use ResMed will repair or replace at its option the defective product or any of its components This Limited Warranty does not cover a any damage caused as a result of improper use abuse modification or alteration of the product b repairs carried out by any service organization that has not been expressly authorized by ResMed to perform such repairs c any damage or contamination due to cigarette pipe cigar or other smoke and d any damage caused by water being spilled on or into an electronic device Warranty is void on product sold or resold outside the region of original purchase Warranty claims on defective product must be made by the initial consumer at the point of purchase This warranty replaces all other expressed or implied warranties including any implied warranty of merchantability or fitness for a particular purpose Some regions or states do not allow limitations on how long an implied warranty lasts so the above limitation may not apply to
12. onnector The DC plug is partially inserted into the back of the device or inserted too slowly 4 Fully insert the DC plug Problem Possible cause Solution A non ResMed power supply Remove the power supply unit and replace with a ResMed power unit is connected to the device supply unit The power supply unit is being Make sure that the power supply unit is free from bedding clothes covered by bedding or other objects that could cover it The following message is displayed on the LCD after you try to update settings or copy data to the SD card Card error please remove SD card and contact service provider SD card is not inserted correctly Ensure that the SD card is inserted correctly You may have removed the Reinsert the SD card and wait for the Home screen or the SD card before settings were Settings updated successfully press any key message to copied to the device appear on the LCD Note This message only appears once If you re insert the SD card after you have updated your settings the message will not be re displayed The following message is NOT displayed on the LCD after you try to update the settings using the SD card Settings updated successfully press any key The settings were not updated Contact your clinician service provider immediately Alarms If the system has not been properly assembled the device will trigger an alarm Check that the air tubing has been properly attached to the device and mask
13. rding or Standard air to EN ISO 17510 1 2009 ubing and H5i Power level CPAP mode With SlimLine air 34 dBA with uncertainty of 2 dBA as measured according ubing to EN ISO 17510 1 2009 With Standard air 35 dBA with uncertainty of 2 dBA as measured according ubing to EN ISO 17510 1 2009 With either SlimLine 36 dBA with uncertainty of 2 dBA as measured according or Standard air to EN ISO 17510 1 2009 tubing and H5i Low nominal 56 dBA Medium nominal 68 dBA High nominal 80 dBA English 9 Supplemental Recommended maximum supplemental oxygen flow 15 L min CPAP S ST T oxygen PAC 4 L min iVAPS mode Air tubing technical specifications Air tubing Material Length Inner diameter ClimateLine heated air tubing Flexible plastic and electrical 2m 15mm components ClimateLine heated air Flexible plastic and electrical 1 9m 19mm tubing components SlimLine air tubing Flexible plastic 1 8m 15mm Standard air tubing Flexible plastic 2m 19mm 3 m air tubing Flexible plastic 3m 19mm Heated air tubing temperature cut out lt 41 C Notes The manufacturer reserves the right to change these specifications without notice The temperature and relative humidity settings displayed for Climate Control are not measured values Check with your clinician service provider before using the SlimLine air tubing with devices other than the S9 or H5i The electrical connector end of the heated air tubing is only compatible wi
14. scular volume depletion e dehydration cerebrospinal fluid leak recent cranial surgery or trauma English 1 Adverse effects Patients should report unusual chest pain severe headache or increased breathlessness to their prescribing physician An acute upper respiratory tract infection may require temporary discontinuation of treatment The following side effects may arise during the course of therapy with the device drying of the nose mouth or throat nosebleed e bloating e ear or sinus discomfort e eye irritation skin rashes Troubleshooting If there is a problem try the following suggestions If the problem cannot be solved contact your equipment supplier or ResMed Do not attempt to open the device enclosure Problem Possible cause Solution No display Power is not connected Ensure the power cord is connected and the power outlet if available is on The DC plug is partially inserted Fully insert the DC plug into the back of the device or inserted too slowly Insufficient air delivered from the device Ramp time is in use Wait for air pressure to build up or change ramp time Air filter is dirty Replace air filter Air tubing is not connected Check air tubing properly Air tubing is blocked pinched or Unblock or free the air tubing Check the air tubing for punctures punctured Mask and headgear are not Adjust position of mask and headgear positioned correctly 2 Problem Possibl
15. th the H5i air outlet and should not be fitted to the device or mask When using the SlimLine or ClimateLine above 20 cm H20 the device optimum performance may not be reached if used with an antibacterial filter The device performance must be checked prior to prescribing the SlimLine for use with an antibacterial filter The ClimateLine or ClimateLine is designed only for use with the H5i Humidifier performance The following settings have been tested at 22 C ambient temperature Nominal system output AH BTPS Mask pressure cm H20 Setting 3 3 90 10 95 20 95 25 100 a AH Absolute Humidity in mg L 100 100 100 100 b BTPS Body Temperature Pressure Saturated Pneumatic flow path Flow maximum at set pressures Setting 6 OMNAMRWN Setting 3 10 11 5 11 12 Flow sensor Blower Pressure sensor Mask Air tubing H5i Alarm module Device Inlet filter The following are measured at the end of the specified air tubing Pressure cm H20 VPAP ST A and Standard L min 12 16 20 25 200 200 200 200 190 180 170 170 170 170 170 161 VPAP ST A H5i and Standard L min 195 190 184 175 168 144 VPAP ST A and SlimLine L min Setting 6 18 21 18 13 5 VPAP ST A H5i and ClimateLine L min 170 170 170 170 161 125 English 11 Displayed values Value Range Display resolution Pressure sensor at air outlet Mask pressure 2 30 cm H20 0 1 cm H20
16. utions may cause damage and reduce the life of these products Incorrect system setup may result in incorrect mask pressure reading Ensure the system is correctly set up Be careful not to place the device where it can be bumped or where someone is likely to trip over the power cord Make sure that the area around the device is dry and clean and clear of bedding clothes or other objects that could block the air inlet or cover the power supply unit Ensure that the device is protected against water if used outdoors Enclose the device in the S9 travel bag for transport ual Manufacturer ResMed Ltd 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia Distributed by ResMed Corp 9001 Spectrum Center Boulevard San Diego CA 92123 USA EC REP ResMed UK Ltd 96 Milton Park Abingdon Oxfordshire 0X14 4RY UK See www resmed com for other ResMed locations worldwide For patent information see www resmed com ip S9 H5i ClimateLine SlimLine SmartStart and VPAP are trademarks of ResMed Ltd S9 ClimateLine SlimLine SmartStart and VPAP are registered in U S Patent and Trademark Office 2012 ResMed Ltd 368823 1 2012 06 C 0123 Global leaders in sleep respiratory medicine www resme
17. vice is turned off so that unused oxygen does not accumulate within the device enclosure and create a risk of fire Do not leave long lengths of air tubing around the top of your bed It could twist around your head or neck while you are sleeping Do not use electrically conductive or antistatic air tubings Do not use the air tubing if there are any visible signs of damage Only ResMed air tubing and accessories should be used with the device A different type of air tubing or accessory may alter the pressure you actually receive reducing the effectiveness of the treatment Only use the ResMed 90W or 30W power supply unit Use the 90W power supply unit to power the system comprising the device H5i air tubing DC DC converter and battery pack The 30W power supply unit is designed to power the device only and recommended for travelling Only ResMed products are designed to be connected to the module connector port Connecting other devices could damage the device Blocking the air tubing and or air inlet of the device while in operation could lead to overheating of the device English 17 A CAUTIONS Do not open the device enclosure There are no user serviceable parts inside Repairs and servicing should only be performed by an authorised ResMed service agent Do not use bleach chlorine alcohol or aromatic based solutions moisturizing or antibacterial soaps or scented oils to clean the device humidifier or air tubing These sol
18. vironmental conditions Aircraft use Electromagnetic compatibility IEC 60601 1 classification 90W power supply unit Input range 100 240V 50 60Hz 115V 400Hz nominal for aircraft use Typical power consumption 70W 80VA Maximum power consumption 110W 120VA 30W power supply unit Input range 100 240V 50 60Hz 115V 400Hz nominal for aircraft use Typical power consumption 20W 40VA aximum power consumption 36W 75VA 90W DC DC converter Nominal inputs 12V 24V Typical power consumption 70W aximum power consumption 110W Operating temperature 5 C to 35 C Note The air flow for breathing produced by this therapy device can be higher than the temperature of the room Under extreme ambient temperature conditions 40 C the device remains safe Operating humidity 10 to 95 non condensing Operating altitude Sea level to 2 591 m air pressure range 1013 hPa to 738 hPa Storage and transport temperature 20 C to 60 C Storage and transport humidity 10 to 95 non condensing ResMed confirms that the device s meets the Federal Aviation Administration FAA requirements RTCA DO 160 section 21 category M for all phases of air ravel Product complies with all applicable electromagnetic compatibility requirements EMC according to IEC60601 1 2 for residential commercial and light industry environments tis recommended that mobile communication devices are kept at least 1 m away from the device nformation reg
19. you English 15 ResMed shall not be responsible for any incidental or consequential damages claimed to have resulted from the sale installation or use of any ResMed product Some regions or states do not allow the exclusion or limitation of incidental or consequential damages so the above limitation may not apply to you This warranty gives you specific legal rights and you may also have other rights which vary from region to region For further information on your warranty rights contact your local ResMed dealer or ResMed office AN WARNINGS e Read the entire manual before using the device Use the device only as directed by your physician or healthcare provider e Use the device only for the intended use as described in this manual Advice contained in this manual should not supersede instructions given by the prescribing physician If you notice any unexplained changes in the performance of the device if it is making unusual or harsh sounds if the device or the power supply are dropped or mishandled if water is spilled into the enclosure or if the enclosure is broken discontinue use and contact your ResMed Service Center Beware of electrocution Do not immerse the device humidifier power supply or power cord in water In the event of a spill disconnect the device from the power supply and let the parts dry Always unplug the device before cleaning and make sure that all parts are dry before plugging in the device
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