User Guide for OXYTIME models including: Q5, Oxygen Concentrator, Q5 Oxygen Concentrator, Concentrator
Oxytime Q5 Oksijen Konsantratörü | Elmaslar Medikal
8 TaúÕma ya da cihazÕQ kapalÕ oldu÷u durumlarda elektrik fiúiQi prizdeQ çekiQiz. OksijHQ NRQVDQWUDtor kabiQLQi yetkili olma\DQ NLúLOHUe açtÕUmayÕQÕz.
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DocumentDocumentMODEL: Q5 2.6ì-(1.216$175$75.8//$1,0.,/$98=8 2;<*(1&21&(175$72586(5*8,'( "KULLANIMDAN ÖNCE KILA98=8'é..A7/é&(2.8<818=o Please read this manual thoroughly before use of the Device ìì1'(.ì/(5 .218/$5 6$<)$12 1. GENEL BLGLER 6 2. ÖNEML UYARILAR 6 3. KURULUM / KULLANIM 10 4. BAKIM 12 5. ARIZA 16 6. HAVA AKI EMASI 18 7. TEKNK ÖZELLKLER 20 8. AKSESUAR LSTES 20 9. ELEKTRONK BAIIKLIK 22 10. GARANT KOULLARI 26 11. SERTFKALAR 26 12. ÜRETC FRMA - YETKL TEKNK SERVSLER 26 &ì+$=(7ì.(7ì1'(.8//$1,/$16(0%2//(5 'ø..A7.8//$1,0 .øT$3d,ö,1, 2.8<818= h5(7ø0T$5ø+ø h5(7ø&ø)ø50$ 6(5ø12 6,1,),,(.ø30$1, '$0/A<$168<A .$5ù,.2580$ 7øP B 7øP%) A958PA 8<80/8/8ö8 %87$5$)<8.$5, .,5,/,5 (//(7$ù,<,1,= .858787818= .$1&$ø/( 7$ù,10$= :((('ø5(.7ø)/(5ø1( 8<*81ø0+A ('ø/0(/ø'ø5 $7(ù/(<$./$ù0$ 6ø*$5$ødø/0(= 2 &217(176 68%-(&76 3$*(12 1. GENERAL INFORMATION 7 2. SAFETY GUIDELINES 7 3. INSTALLATION / USE 11 4. PREVENTIVE MAINTENANCE 13 5. TROUBLESHOOTING 17 6. AIRFLOW DIAGRAMS 19 7. TECHNICAL CHARACTERISTICS 21 8. LIST OF ACCESSORIES 21 9. ELECTROMAGNETIC IMMUNITY 23 10. GUARANTEE (TERMS & CONDITIONS) 27 11. CERTIFICATES 27 12. 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OksijHQ NRQVDQWUDtor kabiQLQi yetkili olma\DQ NLúLOHUe açtÕUmayÕQÕz. ùD\Ht elektrik voltajÕ deQgesizse "Voltaj Regülatörü" ile oDOÕúWÕUÕQÕ]. LütfeQ Qitelikli, güvHQilir elektirik hattÕ ve pirizi kullDQÕQÕz. Elektrik fiúiQi prizdeQ çÕkarÕrkeQ cihaza asÕlarak ya da kablosXQGaQ çekerek çÕkarmayÕQÕz. CihazÕQ hava açÕklÕklaUÕ ya da di÷er açÕklÕklarÕQdaQ yabaQcÕ QesQeler sokmayÕQÕz. CihazÕQÕzÕ çocuklarÕQ müdahalesiQe karúÕ koruyXQuz. CihazÕ sadece fiúi prizdeQ çekili durumdaykeQ temizleyiQiz. Aksi takdirde hayati tehlike söz koQusudur. Cihaza su kaçÕrmayÕQ ve suya daldÕrmayÕQÕz. Cihaz su ile temas edecek olur ise, fiúiQi prizdeQ çekiQ ve yetkili tekQik servis ile görüúüQüz. Cihaz elektri÷e takÕlÕ ikeQ içiQi açmayÕQÕz. CihazÕQ içiQi sadece yetkili firma açabilir. CihazÕQ içiQde siziQ tamir edebilece÷iQiz hiçbir parça bulXQmamaktadÕr. Nazal kaQülQzü yatak arasÕQGa ya da sDQdalye miQderi gibi bir D÷ÕrlÕ÷ÕQ altÕQGa bÕrakmayÕQÕz. KullDQÕm sÕrasÕQGa oluúabilecek herKDQJi bir rahatsÕzlÕ÷Õ iletemeyecek durumdaki yaúlÕ, bebek veya özürlü hastalarÕQ cihazÕ kullDQÕrkHQ dikkatle gözlHQmesi gerekir. Hastada görüleQ eQ ufak bir rahatsÕzlÕk durumuQda hemeQ doktorXQXzu arayÕQÕz. Cihaz hÕzlÕ yaQmayÕ tetikleyici yüksek saflÕkta oksijeQ sD÷lamaktadÕr. CihazÕQ etraIÕQGa ya da oksijeQ taúÕyaQ malzemelerLQ yaQÕQda sigara içilmesiQH iziQ vermeyiQiz, açÕkta ateú bulXQdurmayÕQÕz. CihazÕQÕzÕQ yaQÕQda ya÷ petrol bazlÕ maddeler ya da gres ya÷Õ bulXQGurmayÕQÕz. Üretici ve satÕcÕ firma cihazÕQ herKDQJi bir úekilde yDQlÕú, gereksiz ya da amaç dÕúÕQGD kullDQÕmÕ sRQrasÕQGa oluúacak sorXQlardaQ ya da belirtilHQ elektrik güvHQlik kurallarÕQa uymayaQ úebeke gerilimleri ile kullDQÕmÕ ile oluúDQ soruQlardaQ sorumlu tutulamaz. CihazlarÕQ kullaQÕmÕ süreciQde kalibrasyoQ ihtiyaçlaUÕ : CihazlarÕQ kullDQÕmÕ esQasÕQGD, her 2000 saatte yada yÕlda bir defa aúD÷Õdaki kalibrasyoQ kRQtrolleriQiQ üretici firma tarafÕQGDQ yapÕlmasÕ gereklidir. D2NVLMHQNRQVDQWUDVyRQX b.OksijeQ akÕú miktaUÕ c. OksijeQ çÕkÕú basÕQcÕ YDQJÕQa KarúÕ AkÕú Kesme Valfi : CihazlarÕmÕzda staQdart olarak mevcut olaQ bu özellik çift korumaya sahiptir. Hem kompresör içerisiQGe buluQaQ termostat, motor sÕcaklÕ÷Õ arttÕ÷ÕQda buQu algÕlar ve motoru durdurur, hem de cihaz içerisiQGe bulXQaQ ikiQci bir termostat, cihaz içi sÕcaklÕ÷Õ sürekli ölçer ve bir yDQJÕQ riski durumuQ da cihazÕQ çalÕúmasÕQÕ durdurur ve alarm verir. Çocuklar, emzireQ DQQHler ve hamileler oksijeQ kRQsDQtratörü cihazÕQÕ mutlaka uzmaQ doktor kRQtrolü altÕQda kullaQmalÕdÕr. OksijHQ koQsaQtratörü kullaQmak içiQ doktor reçetesi gerekir ve yaúam destek Qitesi olarak kullDQÕlmaz. OksijeQ tedavisi her yaútaki haslar içiQ |QHrebilir, fakat oksijeQ tedavisi göreQ tipik hastalar ise 65 yaúÕQGDQ büyükler ve KrRQik Obstrüktif Akci÷Hr HastalÕ÷Õ (KOAH) olDQ hastalardÕr. Hastalar iyi zihiQsel beceriye sahip olmalÕ ve rahatlÕkla iletiúim kurabilmelidir. E÷Hr kullDQÕcÕ rahatsÕzlÕ÷Õ sÕrasÕQGD iletiúim kuramÕyorsa veya kRQsaQtratör deki etiketleri ve kullDQÕFÕ kÕlavuzdaki talimatlarÕ okuyamÕyor veya aQlamÕyorsa o zamaQ cihazÕ bilHQ bir bakÕcÕ gözetimi altÕQGD kullDQmalÕdÕr. OksijeQ kRQsDQtratörü kullDQÕmÕ esQasÕQda bir rahatsÕzlÕk hissedilirse, hastalarÕQ doktorlarÕQa baúYurmlarÕ tavsiye edilir. OlaVÕ bir elektrik kesiQtisi veya kRQsaQtratör cihazÕQÕQ bozulma durumuQa karúÕ hastalarÕQ yedekte oksijeQ kayQD÷Õ bulXQdurmalaUÕ tavsiye edilir. &ihaz ömrü 5 yÕlGÕr ve ömrüQü tamalayaQ ürüQler WEEE (Elektrikli ve ElektroQik EkipmaQ AWÕklDUÕ ) direktifiQe uyguQ imha edilmelidir. 2NVLMHQ WHGDYLVL |QFHVL YH WHGDYL VUHVLQFH RNVLMHQOH X\XPOX RODQ VDGHFH VX ED]OÕ ORV\RQ YH\D PHUKHPOHU NXOODQÕQÕ] <DQJÕQYH\D\DQÕNULVNLQL|QOHPHNLoLQSHWUROYH\D\D÷ED]OÕORV\RQYH\DPHUKHPOHUNXOODQPD\ÕQÕ] <DQJÕQ YH \DQÕN ULVNLQL |QOHPHN LoLQ RNVLMHQ \R÷XQODúWÕUÕFÕQÕQ ED÷ODQWÕ SDUoDODUÕQÕ ED÷ODQWÕODUÕQÕ ERUXODUÕQÕ YH\D GL÷HU DNVHVXDUODUÕQÕ\D÷ODPD\ÕQÕ] %X FLKD]ÕQ D]DPL %(<$1 \NVHNOL÷LQGHQ GDKD \NVHNOLNWH YH\D %(<$1 VÕFDNOÕN DUDOÕ÷Õ VÕFDNOÕ÷ÕQ GÕúÕQGD YH\D D]DPL %(<$1ED÷ÕOQHPLQGHQGDKDID]ODED÷ÕOQHPGHNXOODQÕPÕDNÕúÕKÕ]ÕQÕYHRNVLMHQ\]GHVLQLHWNLOHPHVLYHVRQXoWDWHGDYLQLQ NDOLWHVLQLROXPVX]RODUDNHWNLOHPHVLEHNOHQPHNWHGLU &LKD]ÕQNDEORVXYHKRUWXPXQGDQND\QDNOÕER÷XOPDULVNLOHULQHNDUúÕoRFXNODUGDQELOLQFLYHDNOLPHOHNHVLROPD\DQKDVWDODUGDQX]DNWXWXQX] &LKD]GDNoNYH\XWXODELOLUSDUoDODUÕPHYFXWWXU<XWPDULVNLQHNDUúÕoRFXNODUGDQELOLQFLYHDNOLPHOHNHVLROPD\DQKDVWDODUGDQX]DNWXWXQX] &LKD]ÕQ YH HN SDUoDODUÕQÕQ NXOODQÕP DPDoODUÕ GÕúÕQGD NXOODQÕOPDVÕ VRQXFXQGD ROXúDELOHFHN KDWDODUGDQ UHWLFL VRUXPOX GH÷LOGLU hUHWLFLQLQEHOLUOHGL÷LSDUoDODUÕQGÕúÕQGD\HGHNSDUoDNXOODQÕPÕVRQUDVÕQGDROXúDELOHFHNKDWDODUGDQUHWLFLVRUXPOXGH÷LOGLU .XOODQÕPNÕODYX]XQGDWDQÕPODQPD\DQUQSDUoDODUÕQÕQV|NOPHVLGH÷LúWLULOPHVLIDUNOÕUQOHUOHELUOHúWLULOPHVLKDOLQGHUQ JYHQOL÷LQLQER]XOPDVÕQGDQYHROXúDELOHFHNKDWDODUGDQUHWLFLVRUXPOXGH÷LOGLU &LKD]ÕoRFXNODUGDQYHHYFLOKD\YDQODUGDQX]DNWXWXQX] &LKD]D\QÕSDUoDODUNXOODQÕODUDNELUGHQID]ODKDVWDQÕQNXOODQÕPÕQDX\JXQGH÷LOGLU )DUNOÕKDVWDODUGD\HQLWHNNXOODQÕPOÕNELOHúHQOHULOHNXOODQPDVÕJHUHNPHNWHGLU 8 DuriQg traQsportatioQ or wheQ Qot iQ use XQplug the power supply cord. Do Qot allow uQauthorized persoQ to opeQ the cabiQet of the device. If the electric supply liQe suffers from frequeQt voltage fluctuatioQ, we suggest usiQg Voltage Regulator for the device to avoid uQwaQted damages iQ the seQsitive electroQic parts of the device. Do Qot uQplug the power cable by haQgiQg it oQ the device or by pulliQg the cable. Do Qot leak water oQ the device or emerge the device iQto water. If you thiQk there is a chaQce of water may come iQ coQtact with the device, please uQplug the power cable aQd iQform techQical service. Do Qot opeQ the cabiQet of the device wheQ power cable coQQected. OQly authorized techQical service persoQQel is permitted to opeQ the device. There are Qo parts iQside the device which you caQ repair. Do Qot put the Qasal caQQula uQGer heavy material like bed or cushioQ. Keep the device uQder surveillaQce wheQ used by aged, child or disabled patieQt who may Qot able to iQform aQy malfuQctioQiQg of the device may take place duriQg the treatmeQt. Call your doctor immediately iQ case of slightest disturbaQce seeQ iQ the patieQt duriQg treatmeQt. HEALTHTIME device produce highly coQceQtrated oxygHQ which is Qot flammable but accelerates the combustioQ of material. To avoid all risk of fire do Qot smoke Qearby the device aQd other accessories. HEALTHTIME should be kept away from all flames, iQcaQdesceQt sources aQd sources of heat, as well as combustible products like oil, grease, solveQts, aerosols, etc. The maQufacturer of seller of the device is Qot respoQsible for the problems that may occur due to wroQg, uQQecessary or uQiQtHQded use of the device or use of wroQg electrical voltage which Qot comply with electrical safety rules. CalibratioQ requiremeQt iQ the device duriQg use of the device: DuriQg use of the device every 2000 hours or oQce iQ a year followiQg calibratioQ coQtrols to be doQe bymaQufacturera. OxygeQ CoQceQtrator perceQtage b. OxygeQ Flow rate c. OxygeQ outlet pressure Flow Cut-off Valve AgaiQst Fire: This feature available as staQdard iQ our device has double protectioQ facility. The thermostat located iQ the compressor detect the iQcrease iQ Motor temperature aQd shutdowQ the motor wheQ the temperature reach to a deadliQe aQd a secoQd thermostat located iQside the device coQtiQXRusly measure the temperature iQside the device aQd if aQy fire risk detected immediately stop the device aQd gives aQ alarm. ChildreQ, LactatiQg WomeQ aQd PregQaQt must use the oxygeQ coQceQtrator uQder the coQtrol of specialist doctor. OxygeQ CoQFeQWrator use requires a physiciDQ's prescriptioQ DQd are QRt LQWeQGed for life support use.Although oxygeQ therapy caQ be prescribed for patieQts of all ages, the typical oxygeQ therapy patieQt is older thaQ 65 years of age aQd sufferes from chroQic obstructive pulmoQary disease (COPD). PatieQts typically have good cogQitive abilities aQd must be able to commuQicate easily. If the user is uQable to commuQicate discomfort or uQable to read aQd uQderstaQd the coQceQtrator labeliQg aQd iQstructioQs for use, theQ use is recommeQded oQly uQder the supervisioQ of oQe who caQ. If aQy discomfort is felt while usiQg the coQceQtrator, patieQts are advised to coQtact their doctors. PatieQts are aslo advised to have back-up oxygeQ available iQ the eveQt of a power outage or coQceQtrator failure. .Device lifetime is 5 years. .Should be disposed accordiQg to weee ( Waste Electrical aQd ElectroQic EquipmeQt) Directive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Not 1: 80 MHz ve 800 MHz'de, daha yüksek frekDQs aralÕ÷Õ içLQ olaQ ayÕrma mesafesi uygulaQÕr. Not 2: 150 kHz ile 80 MHz arasÕQGDki ISM (HQGstriyel, bilimsel ve tÕbbi) baQtlarÕ 6.765 MHz ile 6.795 MHz13.553 MHz ile 13.567 MHz26.957 MHz ile 27.283 MHz ve 40.66 MHz ile 40.70 MHz'dir. 150 kHz ile 80 MHz arasÕQGDki amatör radyo EDQtlarÕ 1.8 MHz ile 2.0 MHz, 3.5 MHz ile 4.0 MHz, 5.3 MHz ile 5.4 MHz, 7 MHz ile 7.3 MHz, 10.1 MHz ile 10.15 MHz, 14 MHz ile 14.2 MHz, 18.07 MHz ile 18.17 MHz, 21.0 MHz ile 21.4 MHz, 24.89 MHz ile 24.99 MHz, 28.0 MHz ile 29.7 MHz ve 50.0 MHz ile 54.0 MHz'dir. Not 3: %u y|QHrgeler her koúulda geçerli olmayabilir. ElektromDQyetik yayÕlmabLQalar, QHsQHler ve LQsDQlar tarafÕQGDQ emilim ve yDQsÕtÕlmDGDQ etkilHQir. ,úÕQDQ5) 7HVW %DQWD )UHNDQVÕ 0+] 0+] 6HUYLVD 0RGODV\RQE 0RG 0HVDIH %D÷ÕúÕNOÕN ODV\RQE P 7HVW : 6HYL\HVL ,(& TETRA 400 'DUEH0RGODV\RQXE+] 5)NDEORVX] GMRS 4460, FRS 460 FM c) ±5 kHz sapma 1 kHz SLQüs KDEHUOHúPH /7(%$1', 'DUEH0RGODV\RQXE+] FLKD]ODUÕQD NXWX ED÷ÕúÕNOÕNWHVW GSM 800900, TETRA 800, 'DUEH0RGODV\RQXE+] |]HOOLNOHUL øDEN 820, LTE %DQt 5 GSM 1800, CDMA 1900, 'DUEH0RGODV\RQXE+] GSM 1900, DECT, LTE %DQt1,3,4,25, UMTS %luetooth,WLAN 802.11bgQ, 'DUEH0RGODV\RQXE+] RFID 2450,LTE %DQt 7 WLAN 802.11aQ 'DUEH0RGODV\RQXE+] Not: %$öIùIKLIK TEST SEVøYESø1ø elde etmek gerekli ise, verici aQteQ ile medikal cihaz veya medikal ekipmaQ arasÕQdaki mesafe 1 m'ye kadar düúürülebilir. 1'm test mesafesi IEC 61000'e göre 1 mt test mesafesi iziQverilir. a.%azÕservisler içiQyalQÕzca göQderim frekaQslDUÕGDhil edilmiútir. b. TaúÕyÕcÕsiQyali duty cycle'a sahip kare dalga siQyali ile modüle edilmiútir. c. FM modülasyoQuQa alWHUQDWif olarak, 18 Hz de %50 darbe modülasyoQu kullaQÕlabilir, çüQkü gerçek modülasyoQu temsil edeQ eQ kötü seQaryoyu oluúturur. ø0ALATd,5øSK YÖNETø0øNE göre miQimum ayÕrma mesafesiQi azaltmayÕve azalWÕlmÕú miQimum ayÕrma mesafesiQe uyguQdaha yüksek %AöIùIKLIK TEST SEVøYELE5økullaQmayÕdüúüQmelidir. 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