User manual RESPIRONICS REMSTAR M

[. . . ] 1016452 AM 2/09/06 Important! Fill in the information below when you receive the REMstar® M Series system. Serial No. : _______________________________ (located on the bottom of the device) System Prescribed for: __________________________________________ Date of Purchase or Rental: ______________________________________ Pressure Setting: _____ cm H2O Mask Type: __________________________________________________ Mask Size: ___________________________________________________ If you have any questions concerning the system, contact: · · · Home Care Company: _______________________________________ Telephone Number: _________________________________________ Health Care Professional: _____________________________________ Telephone Number: _________________________________________ Respironics, Inc. 1001 Murry Ridge Lane Murrysville, Pennsylvania 15668-8550 USA Customer Service Telephone Number: 1-800-345-6443 or 1-724-387-4000 The REMstar® M Series system is covered by the following patent: 6, 622, 724. All rights reserved. reply_card1. pdf 9/19/05 10:52:10 AM C M Y CM MY CY CMY K FIRST-CLASS MAIL PERMIT NO. 231 GRAND RAPIDS MN PO BOX 7014 GRAND RAPIDS MN 55744-8029 reply_card2. pdf 9/19/05 11:22:20 AM ® C M Please complete the following or register online at: www. mseries. respironics. com Model #: Product Identification Information (Numbers located on the bottom of the device) Y Serial #: CM MY Name CY Address City Phone ( E-mail Where did you first hear about your M Series device? [. . . ] Refer to the instructions supplied with the DC Power Cord and adapter cable for information on how to operate the device using DC power. 3-6 REMstaR M sERiEs UsER ManUal 3. 5 CoMplEtE assEMbly ExaMplE Figure 3­7 shows an example of how a complete assembly will look, with breathing circuit connected and power applied to the device. figURE 3­7 final assEMbly ExaMplE Figure 3­8 shows an example of how you should route your tubing and situate your device on your night stand for the best setup possible. This will help prevent the device from falling off your night stand or table. figURE 3­8 RECoMMEndEd dEviCE and tUbing plaCEMEnt REMstaR M sERiEs UsER ManUal 3-7 3-8 REMstaR M sERiEs UsER ManUal ChaptER 4: dEviCE opERation This chapter explains how to start the device and change the settings. 4. 1 1. staRting thE dEviCE Plug the device in to an AC or DC power source. The number that appears on your screen will be different from the number shown below. figURE 4­1 softWaRE vERsion sCREEn 2. The next screen to appear is the Standby screen, which displays the cumulative therapy hours. When you first begin using this device, the number shown will be zero, but as you use it, the number shown here will increase. Your provider may ask you for this number. figURE 4­2 standby sCREEn 3. When you press the Start/Stop button displays, as shown below. to turn on the airflow, the Active Display screen figURE 4­3 thE aCtivE display--WithoUt RaMp (lEft) and With RaMp (Right) REMstaR M sERiEs UsER ManUal 4-1 The Active Display screen shows the prescribed or ramping pressure. If the ramp feature is enabled by your health care provider, the Ramp symbol also appears as described below: syMbol dEsCRiption If the Ramp feature is enabled, you can initiate it by pressing the Ramp button. When the ramp function is active, the Ramp symbol displays on the Active Display screen, as shown above. Asmallamountofmaskleakisnormalandacceptable. Correctlargemask leaksoreyeirritationfromanairleakassoonaspossible. Note: 6. If you are using the device while sleeping, try placing the tubing from the device over your headboard. Ifyouarehavingtroublewithyourmask, refertotheinstructionssuppliedwith themask. Note: 4. 2 Using thE RaMp fEatURE The optional Ramp feature can be enabled or disabled by your home care provider. This feature reduces the air pressure when you are trying to fall asleep. Then it gradually increases (ramps) the pressure until your prescription setting is reached, allowing you to fall asleep more comfortably. If ramp is enabled on your device, after you turn on the airflow, press the Ramp button the top of the device. Note: Iftherampfeatureisdisabled, nothingwillhappenwhenyoupresstheRamp button. on 4-2 REMstaR M sERiEs UsER ManUal 4. 3 Changing thE dEviCE sEttings You can view the prescribed or ramping pressure on the Active Display screen, as well as the following information on the Patient Data screens: · · · · · Hours of Patient Use Session Counter (number of sessions greater than 4 hours) Compliance Check Value Altitude Ramp starting pressure (if enabled by your home care provider) You can view your therapy usage hours on the Standby screeneachtime youturnonthedevice. Additionally, you can view and modify the following settings on the Patient Setup screens: Note: REMstaR M sERiEs UsER ManUal 4-3 4. 3. 1 navigating thE display sCREEns Use the button to navigate to the next screen and the button to navigate to the previous screen. Use the Plus (+) and Minus (­) buttons to adjust the settings on the Patient screens. 4. 3. 1. 1 Press the screens. viEWing thE patiEnt data sCREEns button to enter the Data screens. Figure 4­5 shows how to navigate the Patient Data Press To Enter These Screens Standby Screen (showing therapy hours) Hours of Patient Use View Screen >4 Compliance Check Value View Screen Session Counter View Screen figURE 4­4 navigating thE patiEnt data sCREEns Press the button to scroll forward through these screens, or press the through the screens in the reverse order. From any of these screens, press the Start/Stop button Note: button to scroll to return to the Standby screen. Afteroneminuteofinactivity, theDatamodeautomaticallytimesoutand returnstotheStandbyscreen. 4-4 REMstaR M sERiEs UsER ManUal 1. Hours of Patent Use Vew Screen This screen shows you the total number of hours that the blower has been active. Your home care provider may periodically ask for this information. >4 2. Sesson Counter Vew Screen This screen shows you the number of sessions greater than four hours. Your home care provider may periodically ask for this information. 3. Complance Check Value Vew Screen This screen shows you the Compliance Check Value, which typically is a different number from the one shown here. Your home care provider may periodically ask for this information. REMstaR M sERiEs UsER ManUal 4-5 4. 3. 1. 2 viEWing and Modifying thE patiEnt sEtUp sCREEns Press the button to enter the Setup screens. The figure below shows how to navigate the Patient Setup screens. Press To Enter These Screens Standby Screen (showing therapy hours) Ramp Start Pressure Adjustment Screen* Altitude Adjustment Screen figURE 4­5 navigating thE patiEnt sEtUp sCREEns. [. . . ] iMMUnity tEst Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 iEC 60601 tEst lEvEl 3 A/m CoMplianCE lEvEl 3 A/m ElECtRoMagnEtiC EnviRonMEnt gUidanCE Power frequency magnetic fields should be at levels characteristic of a typical location in a typical hospital or home environment. Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Conducted RF IEC 61000-4-6 Radiated RF IEC 61000-4-3 3 Vrms 150 kHz to 80 MHz 3 V/m 80 MHz to 2. 5 GHz 3 Vrms 3 V/m Recommended separation distance d = 1. 2 P d = 1. 2 P 80 MHz to 800 MHz d = 2. 3 P 800 MHz to 2. 5 GHz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each frequency range. b Interference may occur in the vicinity of equipment marked with the following symbol: NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. [. . . ]