Omron HBP-1300 Bedienungsanleitung

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Richtige Gebrauchsanleitung

Die Vorschriften verpflichten den Verkäufer zur Übertragung der Gebrauchsanleitung Omron HBP-1300 an den Erwerber, zusammen mit der Ware. Eine fehlende Anleitung oder falsche Informationen, die dem Verbraucher übertragen werden, bilden eine Grundlage für eine Reklamation aufgrund Unstimmigkeit des Geräts mit dem Vertrag. Rechtsmäßig lässt man das Anfügen einer Gebrauchsanleitung in anderer Form als Papierform zu, was letztens sehr oft genutzt wird, indem man eine grafische oder elektronische Anleitung von Omron HBP-1300, sowie Anleitungsvideos für Nutzer beifügt. Die Bedingung ist, dass ihre Form leserlich und verständlich ist.

Was ist eine Gebrauchsanleitung?

Das Wort kommt vom lateinischen „instructio”, d.h. ordnen. Demnach kann man in der Anleitung Omron HBP-1300 die Beschreibung der Etappen der Vorgehensweisen finden. Das Ziel der Anleitung ist die Belehrung, Vereinfachung des Starts, der Nutzung des Geräts oder auch der Ausführung bestimmter Tätigkeiten. Die Anleitung ist eine Sammlung von Informationen über ein Gegenstand/eine Dienstleistung, ein Hinweis.

Leider widmen nicht viele Nutzer ihre Zeit der Gebrauchsanleitung Omron HBP-1300. Eine gute Gebrauchsanleitung erlaubt nicht nur eine Reihe zusätzlicher Funktionen des gekauften Geräts kennenzulernen, sondern hilft dabei viele Fehler zu vermeiden.

Was sollte also eine ideale Gebrauchsanleitung beinhalten?

Die Gebrauchsanleitung Omron HBP-1300 sollte vor allem folgendes enthalten:
- Informationen über technische Daten des Geräts Omron HBP-1300
- Den Namen des Produzenten und das Produktionsjahr des Geräts Omron HBP-1300
- Grundsätze der Bedienung, Regulierung und Wartung des Geräts Omron HBP-1300
- Sicherheitszeichen und Zertifikate, die die Übereinstimmung mit entsprechenden Normen bestätigen

Warum lesen wir keine Gebrauchsanleitungen?

Der Grund dafür ist die fehlende Zeit und die Sicherheit, was die bestimmten Funktionen der gekauften Geräte angeht. Leider ist das Anschließen und Starten von Omron HBP-1300 zu wenig. Eine Anleitung beinhaltet eine Reihe von Hinweisen bezüglich bestimmter Funktionen, Sicherheitsgrundsätze, Wartungsarten (sogar das, welche Mittel man benutzen sollte), eventueller Fehler von Omron HBP-1300 und Lösungsarten für Probleme, die während der Nutzung auftreten könnten. Immerhin kann man in der Gebrauchsanleitung die Kontaktnummer zum Service Omron finden, wenn die vorgeschlagenen Lösungen nicht wirksam sind. Aktuell erfreuen sich Anleitungen in Form von interessanten Animationen oder Videoanleitungen an Popularität, die den Nutzer besser ansprechen als eine Broschüre. Diese Art von Anleitung gibt garantiert, dass der Nutzer sich das ganze Video anschaut, ohne die spezifizierten und komplizierten technischen Beschreibungen von Omron HBP-1300 zu überspringen, wie es bei der Papierform passiert.

Warum sollte man Gebrauchsanleitungen lesen?

In der Gebrauchsanleitung finden wir vor allem die Antwort über den Bau sowie die Möglichkeiten des Geräts Omron HBP-1300, über die Nutzung bestimmter Accessoires und eine Reihe von Informationen, die erlauben, jegliche Funktionen und Bequemlichkeiten zu nutzen.

Nach dem gelungenen Kauf des Geräts, sollte man einige Zeit für das Kennenlernen jedes Teils der Anleitung von Omron HBP-1300 widmen. Aktuell sind sie genau vorbereitet oder übersetzt, damit sie nicht nur verständlich für die Nutzer sind, aber auch ihre grundliegende Hilfs-Informations-Funktion erfüllen.

Inhaltsverzeichnis der Gebrauchsanleitungen

  • Seite 1

    Profe ssional Blood Pressur e Monitor HBP-1300 • Instruction Manual • Mode d’em ploi • Gebrauchsanweisung • Manuale di istruzion i • Manual de instrucciones • Gebruiksaanwijzing •             • Kullanm Klavuzu EN FR DE IT ES IM-HB P-13 00-E -01-0 2/20[...]

  • Seite 2

    Content s Intr oduction Intend ed Use ........ ................. ........... ................. ........... ................. ........... ................. .... 1 Exemp tions ........... ........... ................. ........... ................. ........... ................. ........... .......... 1 Notes o n Safety ............... ................[...]

  • Seite 3

    1 EN Introduction Intended Use Medical Purpos e The device is a digital m onitor intended for use in measuring blood pressure and pulse rate in adult and pediatric patient population with arm circumference ranging from 12 cm to 50 cm (from 5 inches to 20 inches). Intend ed User This device should be used by a medical prof essional. Pa tie n t Po pu[...]

  • Seite 4

    2 Notes on Safe ty The warning signs and symbol exa mples indicated below are intended t o ensure safe us e of the product and prevent damage and injury to you and others. The signs and symbols are explained below . Safety Symbols used in this Inst ruction Manual Wa r n i n g Ind icates the matte rs in which dea th or severe bodily damage may arise[...]

  • Seite 5

    3 EN W arnings and Cautions Usage warni ngs and cau tions Setup Wa r n i n g Caution Do not use t he cuff or AC adapt er to lif t the unit, it c an also caus e the unit to m alfunction. If the unit has brok en dow n, contact OMRON HEAL THCARE. Do not use in combination w ith a hyperbaric oxygen therapy device, or in an environment where combustible[...]

  • Seite 6

    4 Before use / during use Wa r n i n g The unit complies with the EMC st anda rd (IEC60601-1-2). As such, it can be used simult aneously with multiple medical instrument s. However , if instruments t hat generate noise such as an electric scalpel or a microwave therapy device are near the unit, check the operation of the uni t during and after use [...]

  • Seite 7

    5 EN Caution Before using the unit, verify that none of t he following apply to t he pati ent: - Poor peripheral circulation, noticeably low blood pressure, or low body temperature (there will be low blood f low to the measurement position) - The p atient uses an artificial heart and lung (there will be no pulse) -A n S p O 2 sensor and the c uf f [...]

  • Seite 8

    6 Cleanin g Wa r n i n g Cauti on Maintena nce a nd insp ection Wa r n i n g When cleaning the unit, t urn off the power and disconnect the AC adapter from the unit. After cl eaning the unit, make sure it is completely dry before connecting to a power outlet. Do not spray , pour , or spill liquids into or on to the unit, acce ssories, connect ors, [...]

  • Seite 9

    7 EN W arnings and c autions for safe measurem ent Recha rgeab le b atte ry Wa r n i n g Caution If battery fluid comes in contact with the eye, immediately flush with copious amounts of water . Do not rub. Seek m edical attention immediately . Do not use t he battery pack in any other device besides this unit . Do not throw into flame, disassemble[...]

  • Seite 10

    8 Non-Inva sive Bloo d Pre ssure (NI BP) meas ure ment Wa r n i n g Cauti on If a cuf f is used on a pat ient with an inf ection, treat the cuff as medical waste, or disinfect before reuse. If frequently performing NIBP measurement using a cuf f over an extended period of time, periodically check the patient’ s circulation. In addition, wrap t he[...]

  • Seite 11

    9 EN Note: Setup • Read and understand the manual for each optional accessory . This manual does not contain cautionary inf ormation for optional acces sory . • Exercise caution with the cables and arrange so t hat the pat ient does not become entangled or bound. Bef ore us e / du r in g use • Check the following af ter turning on the power: [...]

  • Seite 12

    10 Using the Unit Component s of the Product Before using the unit, make sure that no accessories are missing and that the unit and accessories are not damaged. If an accessory is missing or there is damage, please contact OMRON HEAL THCARE. Main unit S tand ard Medi cal Accesso r ies • GS CUFF L (32 - 42 cm)/ M (22 - 32 cm) • AC ad apter Other[...]

  • Seite 13

    11 EN Optiona l Medi cal Acce ssori es (within the scope of EC Medical Device Directive 93/42/EEC) * UK plug type AC AD APTER-UK 1600 (9994843-9) Caution Only O MRON G S CUFF can be us ed with this device. Features of the Produc t The OMRON HBP- 1300 is an af f ordable professional blood pressure unit that is clinical ly proven accurate and provide[...]

  • Seite 14

    12 Features / Functions of Unit Front an d back of un it Meanin g of t he Sy mbols 1 [ST A RT/STOP ] butto n (Pow er ON /OFF) Power ON / Measure blood pressure Pres s when the p ower is of f to tur n on th e power and st art blood pre ssure measur ement. During infla tion or measu rement, press to stop. Powe r OFF Hold down at least 3 sec onds to t[...]

  • Seite 15

    13 EN LCD Display * O nly when the battery is inst alled. 1 SYS Displays sys tolic bloo d pressure . 2 DIA Displays diast o lic blood pres sure. 3 Pulse Displays the pulse rate. 4 Puls e synchronizatio n icon Flashes in syn chroniz ation wit h the pulse duri ng measur ement. 5 Irre gular pul se wave icon Light s in the meas urement result dis play [...]

  • Seite 16

    14 Inst a lling the Battery Pac k Cauti on Do not short the positive and negative terminals of the battery pack with a wire or other metal object. If battery fluid comes into cont ac t with t he skin or clothes, immediately rinse with wat er . 1. Make su re the AC adap ter has been d isconn ected . 2. Remove the two screws from the top of the rear [...]

  • Seite 17

    15 EN Battery ch arging Battery lev el Connecting the AC Adapter AC power V erify that the power out let supplies the specified voltage and frequenc y (100 - 240 V AC, 50/60 Hz). Connect the AC adapter to the DC jack on the unit and the power outlet. Note: When the ba tt ery pack is i nst alle d If there is no pr oblem with the f ollowing. - A C ad[...]

  • Seite 18

    16 Syste m Settings The syst em settings are divided into t wo modes, “ Menu Mode” and “Ut ility Mode”. Menu Mode “Menu Mo de” al low s yo u to co nfig ure t he “I niti al In flatio n Pr ess ure V alue ” an d “Au sculta tion Mode ” set tin gs. 1. Press the [MODE] butt on. The “Initial Inflation Pressure V a lue” setting scre[...]

  • Seite 19

    17 EN Utility Mode “Utility M ode” a llows y ou to con figure th e “Auto Powe r Off” and “Pr essure Accurac y Confir mation ” setting. 1. Con fir m tha t th e d evi ce i s swit ched o f f. If the power i s on, hold down t he [ST ART/STOP] button for at least 3 seconds t o turn of f the power . 2. Hold down the [MODE] butto n until the ?[...]

  • Seite 20

    18 Non-Invasive Blood Press ure (NIBP) Measurement Non-Invasi ve Pressure Measur ement Principle s Oscillometric method The beat in t he pulsation generated by the contraction of the heart is captured as t he pressure inside the cuff to measure the blood pressure. If t he cuff wrapped around t he upper arm is pressurized suf ficiently , the blood f[...]

  • Seite 21

    19 EN Cuff Selection and Connection Selectin g the cuff Caution • D o not us e the cuff if it is da maged or has ho les. • U se the appropriate cu ff size to ensur e correct m easurements. If a cuff that is too larg e is used, the measured blood press ure value tends to be lower t han the actual blood pressure . If a cuf f that is too small is [...]

  • Seite 22

    20 Applying the Cuff to the Patient 1. Wrap on a bare arm or over thin clothing. Wrap t he cuff on a bare arm or over thin clothi n g . Thick clothing o r a rolled up sleeve will cause inaccurate blood pressure measu rements. The device can be used on either the right or left arm. 2. A lign the ar tery mark “I NDEX AR TER Y” with the br achial [...]

  • Seite 23

    21 EN Caution Make sure the cuff is wrapped in the correct arm position an d is at the same he ight as the h eart. A dif ference of 10 cm (4 inches) in hei ght may cause a variation in the blood pres sure value of up to 7 - 8 mmHg. Note: • I f meas urement is dif fic ult due to arrhyt hmia, use a di f feren t blood pressure measure ment met hod. [...]

  • Seite 24

    22 Irregula r pulse w ave detect ion function If the pulse wav e interval becom es irregular dur ing measurem ent, the irregular puls e wave det ection icon will light to notify you. Body m ovemen t detectio n function If body m ovement is d etected during measure ment, deflation st ops for 5 seco nds. T he irregular pulse wave icon appears in the [...]

  • Seite 25

    23 EN S topping the Meas urement T o stop measurement while measurement is in progress, press [ST ART/STOP] button. Displayi ng Last Reading The previous meas urement value (systolic blood pressure, diastolic blood pres sure, and pulse rat e) and whether or not an irregular pulse wave was det ected can be displayed. In t he case of auscultation mea[...]

  • Seite 26

    24 Maintenance Maintenance In spection and Safe ty Management The HBP-1300 must be maintained to ensure func tionality and to secure the saf ety of patien t s and operators. Daily checks and maintenance should be per formed b y the operator . (page 25) In addition, qualified personnel are necessary to maint ain the performance and the sa fety , and[...]

  • Seite 27

    25 EN Check be fore Use Before cond ucting safety checks, be su re to imple ment the items in the “Cleaning of the D evice” and “A ccessory Care” sect ions. (page 24) Before turning on t he power Before t urning on the power , check f or the following External appear ance Q The device or accessories are not deformed due to falling or other [...]

  • Seite 28

    26 T roubleshooting The power do es not turn on Cause S olutio n If the un it is being powered by the bat tery , the batte ry is not ins ta lled or the charge is depl eted. Insert ba ttery or replace with a ne w batter y (page 14 ). Inte rnal part f ailu re Discon nect the AC ad apter , remo ve t he b attery , and conta ct OMRON HE AL THCAR E. • [...]

  • Seite 29

    27 EN Abnormal measurement value Cause / solu tion The causes below are possi ble. Chec k th e pat ient by pa lp ation and th en repeat measure ment. • Body movement (chil ls or oth er tremblin g) • Arrhythmia. • Noi se in the c uff - A nearb y pe rson touc hed t he p atient. - Cardiac mass age was bei ng performed. The meas urement va lue is[...]

  • Seite 30

    28 List of Error Codes The alarm lamp flashes when a medi um-priority alarm occur s, and light s steadily when a l ow-priority alarm occurs. T o clear an alarm, press any button. Q If a low-priority alarm and a medium -priority alarm occur at the sam e time, the medium-priority alarm is displayed. If the alarms are the same priority level, the erro[...]

  • Seite 31

    29 EN Other problem s Disposal Descriptio n As there is a risk of environmental pollution, follow y our applicable national and local legal regula tions regarding dispos al or recy cling of this equipment and batteries. The main constituents of each p a rt are li sted in the t able below . As there is a risk of inf ection, do not recycle patient at[...]

  • Seite 32

    30 S peci ficat ions Factory Default Settings Factory default settings and backup are as shown below . Backup : Setting i s retained even i f the power is interrupted. : Reverts t o factory default setting if the power i s turned off. T echnica l Specifications: HBP-130 0 Main unit Power sup ply Sett ing Pr ess ure V al ue Setti ngs Factory Se ttin[...]

  • Seite 33

    31 EN Environme ntal Conditions Non-Invas ive Blood Pressure (NI B P) * C omparison with auscultation method performed by a trained prof essional. DIA determined by the auscultation method is “K5”. Note: S pecifications m ay be c hanged without prior notice. This blood pressure monitor fulfils the requirements of the EC directive 93/42/EEC (Med[...]

  • Seite 34

    32 Important information regarding Elec tro Magnet ic Compatibility (EMC ) With the increased number of electronic devices such as PC’ s and mobile (cellular) telephones, medical devices in use may be susceptible to electromagnetic interference from other devices. Electromagnetic interference may result in incorrec t operation of t he medical de [...]

  • Seite 35

    33 EN Manufacturer ’ s Declarat ion The HBP -1300 is inte nded for use in the electromag netic environm ent specified below . The cust omer or the user of the HBP- 1300 should ass ure that it is used in such an environment . Electromagnetic E missions: (IEC6 0601-1-2) Electromagnetic I mmunity: (IEC6 0601-1-2) Emissi on T est Compliance Elec trom[...]

  • Seite 36

    34 Immunity test IEC60601-1-2 test level Compliance level Electromagneti c environment - guidance Conduct ed RF IEC 61000-4 -6 Radiat ed RF IEC 61000-4 -3 3 V rms 150 kHz to 80 MH z 80% A M ( 2H z) 3V / m 80 MH z to 2.5 GH z 80% A M ( 2H z) 3 V rms 3 V/m Port able and mobile RF communicat ions equipmen t shoul d be used no close r to any p art of t[...]

  • Seite 37

    35 EN Recomm ended Separation Distances: Recommended separation dist anc e between port able and mobile RF commun ications equipment and the HBP-1300 The HBP- 1300 is intend ed for u se in an elec troma gnetic en v ironme nt in whic h radia ted RF dis turban ces are co ntrolled . The customer or the user of the HBP-1 300 can help preve nt elec trom[...]

  • Seite 38

    Made in C hina Manufacturer OMRON HEAL THCA RE Co., Lt d. 53, Kunotsubo, T era do-cho, Muko, Kyoto, 617-0002 JAP AN EU-rep resent ative OMRON HE AL THCARE EUROPE B .V . Scorpius 33, 2132 LR Hoofddorp, THE NETHERLANDS www .omron-healthcare. com Product ion facility OMRON (DALIAN) CO., L TD. Dalian, CHINA S ubs id ia ry OMRON HEAL THCA RE UK L TD. Op[...]