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District, 528437 Zhongshan, Guangdong, Čína Zástupce pro EU: Medical Device Safety Service GmbH Schiffgraben 41, 30175 Hannover, Německo Dovozce pro ČR, Celimed s.r.o. autorizovaný servis: Sociální péče 3487/5a, 400 11 Ústí nad Labem, Česká republika Pozáruční servis – tel.: +420 475 208 180 e-mail: info@celimed.cz www.celimed.cz...
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District, 528437 Zhongshan, Guangdong, Čína Zástupca pre EÚ: Medical Device Safety Service GmbH Schiffgraben 41, 30175 Hannover, Nemecko Dovozca pre SR, Celimed s.r.o. autorizovaný servis: Pri majeri 22 831 06 Bratislava, Slovenská Republika Servis: 02 4468 1249 e-mail: info@celimed.sk www.celimed.sk...
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Adapter Típus: BLJ06L050100U-V Bemenet: 100–240 V, 50–60 Hz, 0,2A max 1000 mA , 5,0 W...
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EMC ÚTMUTATÓ Útmutató és gyártói nyilatkozat – elektromágneses kisugárzás Kibocs t si vizsg lat Megfelel s CISPR 11 [ B ] oszt ly CISPR 11 A oszt ly IEC 61000-3-2 Fesz lts IEC 61000-3-3...
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2. táblázat Útmutató és gyártói nyilatkozat -– IEC 60601-1-2 Immunitásvizsgálat Megfelelési szint Vizsgálati szint ±8 kV érintkezés ±8 kV érintkezés kisülés (ESD) ±2 kV, IEC 61000-4-2 ±2 kV a tápvezetékek esetében ±2 kV a tápvezetékek esetében Gyors elektromos tranziens/kitörés ±1 kV jel bemenet/kimenet Nem alkalmazható...
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3. táblázat Útmutató és gyártói nyilatkozat – Kibocsátott RF Vizsgálati Sáv (MHz) Szolgáltatás Maximális Távolság IEC 60601-1-2 teljesítmé Vizsgálati szint ési szint IEC61000-4-3 (V/m) (Vizsgálati (V/m) a (MHz) ny (W) 380-390 TETRA 400 Impulzus 18 Hz E a vezeték FM ± 5k Hz 430-470 GMRS 460, nélküli...
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District, 528437 Zhongshan, Guangdong, Kína EU-kepviselet: Medical Device Safety Service GmbH Schiffgraben 41, 30175 Hannover, Németország Forgalmazo / HU Celimed s.r.o. importer Sociální péče 3487/5a, 400 11 Ústí nad Labem, Cseh Köztársaság Garancia utáni szerviz – tel.: +420 475 208 180 e-mail: info@celimed.cz www.celimed.cz...
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CAUTION * This device is intended for indoor, home use. * This device is not intended for public use. * This device is portable, but it is not intended for use during patient transport. * This device is not suitable for continuous monitoring during medical emergencies or operations. * This device is intended for no-invasive measuring and monitoring of arterial blood pressure.
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CAUTION * Warning: This device is not AP/APG equipment. Do not use the device where flammable anesthetic are present, or in environments mixture with air of with oxygen or nitrous oxide. * The device contains sensitive electronic components.To avoid measurement errors, avoid taking blood pressure measurements near a strong electromagnetic field radiated interference signal or electrical fast transient/burst signal.
Setting the Date and Time It is important to set the clock before using your blood pressure is stored in the memory. (year: 2021—2050, Time format: 12H/24H)
What are systolic pressure and diastolic pressure? Systolic Diastolic blood entering blood discharging vein artery press relax What is the standard blood pressure classification? CAUTION Irregular Heartbeat Detector CAUTION...
Why does my blood pressure fluctuate throughout the day? Why do I get different blood pressure at home compared to the hospital? Is the result the same if measuring on the right arm?
TROUBLE SHOOTING If any abnormality arises during use, please check the following points: PROBLEM SYMPTOM CHECK THIS REMEDY No power High power batteries Error message Warning message...
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Power supply Display mode Measurement mode Measurement range Accuracy Normal working condition Storage & transportation condition Measurement perimeter of the upper arm Weight External dimensions Attachment Mode of operation Degree of protection Protection against ingress of water Device Classification Software Version...
Athorized Component Please use the TRANSTEK authorized adapter. Adapter Type: BLJ06L050100U-V Input: 100-240V, 50-60Hz, 0.2A max 1000 mA Output: Limited Warranty The manufacturer provides a 2-year warranty on this product (main unit) from Contact Information the date of purchase.
EMC GUIDANCE EMC Guidance The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments. Warning: Don’t be near the active HF surgical equipment and the RF shielded room of an ME system for magnetic resonance imaging, where the intensity of EM disturbances is high. Warning: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation.
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Table 2 Guidance and manufacturer’s declaration – electromagnetic Immunity IEC 60601-1-2 Immunity Test Compliance level Test level Electrostatic ±8 kV contact ±8 kV contact discharge (ESD) ±2 kV, ±4 kV, ±8 kV, ±15 kV air ±2 kV, ±4 kV, ±8 kV, ±15 kV air IEC 61000-4-2 ±2 kV for power supply lines ±2 kV for power supply lines...
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Table 3 Guidance and manufacturer’s declaration - electromagnetic Immunity Compliance Radiated RF Test Band Service Modulation Distance Maximum 60601-1-2 level IEC61000-4-3 Frequency (MHz) Power Test Level (V/m) (MHz) (Test (V/m) specifications 380-390 Pulse TETRA modulation ENCLOSURE 18 Hz PORT IMMUNITY to 430-470 GMRS 460, FM ±...
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China Representative for Medical Device Safety Service GmbH the EU: Schiffgraben 41, 30175 Hannover, Germany Importer for the Celimed s.r.o. CR, authorized Sociální péče 3487/5a, service: 400 11 Ústí nad Labem, Czech Republic Post-warranty service – tel.: +420 475 208 180 e-mail: info@celimed.cz www.celimed.cz...