sĞƌƐŝŽŶ͗ ϭ͘Ϭ User Manual Blood Pressure Monitor Model: TMB-1490-BHJ Arm Type MEM O RY M S S TA R S TO T P 'ƵĂŶŐĚŽŶŐ dƌĂŶƐƚĞŬ DĞĚŝĐĂů ůĞĐƚƌŽŶŝĐƐ Ž͕͘ >ƚĚ͘ ŽŶĞ ͕ EŽ͘ϭϬϱ͕ ŽŶŐůŝ ZŽĂĚ͕ dŽƌĐŚ ĞǀĞůŽƉŵĞŶƚ ŝƐƚƌŝĐƚ͕ ŚŽŶŐƐŚĂŶ͕ ϱϮϴϰϯϳ͕ 'ƵĂŶŐĚŽŶŐ͕ ŚŝŶĂ dŚĂŶŬ LJŽƵ ĨŽƌ ƐĞůĞĐƟŶŐ dƌĂŶƐƚĞŬ ůŽŽĚ WƌĞƐƐƵƌĞ DŽŶŝƚŽƌ͘ WůĞĂƐĞ ƌĞĂĚ ƚŚĞ ƵƐĞƌ ŵĂŶƵĂů ĐĂƌĞĨƵůůLJ ĂŶĚ ƚŚŽƌŽƵŐŚůLJ ƐŽ ĂƐ ƚŽ ĞŶƐƵƌĞ ƚŚĞ ƐĂĨĞ ƵƐĂŐĞ ŽĨ ƚŚŝƐ ƉƌŽĚƵĐƚ͘ <ĞĞƉ ƚŚŝƐ ŵĂŶƵĂů ĨŽƌ ĨƵƌƚŚĞƌ ƌĞĨĞƌĞŶĐĞ ŝŶ ĐĂƐĞ ĂŶLJ ŝƐƐƵĞƐ ĂƌŝƐĞ͘
CATALOGUE Table of Contents IEdZK h d/KE͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘Ϯ 'ĞŶĞƌĂů ĞƐĐƌŝƉƟŽŶ /ŶĚŝĐĂƟŽŶƐ ĨŽƌ hƐĞ ŽŶƚƌĂŝŶĚŝĐĂƟŽŶƐ DĞĂƐƵƌĞŵĞŶƚ WƌŝŶĐŝƉůĞ ^ĂĨĞƚLJ /ŶĨŽƌŵĂƟŽŶ > ŝƐƉůĂLJ ^ŝŐŶĂů DŽŶŝƚŽƌ ŽŵƉŽŶĞŶƚƐ >ŝƐƚ &KZ zKh ^d Zd͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘͘ϵ dŚĞ ŚŽŝĐĞ ŽĨ WŽǁĞƌ ^ƵƉƉůLJ /ŶƐƚĂůůŝŶŐ ĂŶĚ ZĞƉůĂ
INTRODUCTION INTRODUCTION General Description Safety Information dŚŝƐ ƉƌŽĚƵĐƚ ĨĞĂƚƵƌĞƐ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ŵĞĂƐƵƌĞŵĞŶƚ͕ ƉƵůƐĞ ƌĂƚĞ ŵĞĂƐƵƌĞŵĞŶƚ ĂŶĚ ƚŚĞ ƌĞƐƵůƚ ƐƚŽƌĂŐĞ͘ dŚĞ ĚĞƐŝŐŶ ƉƌŽǀŝĚĞƐ LJŽƵ ǁŝƚŚ ƚǁŽ LJĞĂƌƐ ŽĨ ƌĞůŝĂďůĞ ƐĞƌǀŝĐĞ͘ ZĞĂĚŝŶŐƐ ƚĂŬĞŶ ďLJ ƚŚŝƐ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ŵŽŶŝƚŽƌ dD ͲϭϰϵϬͲ ,: ŝƐ ĞƋƵŝǀĂůĞŶƚ ƚŽ ƚŚŽƐĞ ŽďƚĂŝŶĞĚ ďLJ Ă ƚƌĂŝŶĞĚ ŽďƐĞƌǀĞƌ ƵƐŝŶŐ ƚŚĞ ĐƵī ĂŶĚ ƐƚĞƚŚŽƐĐŽƉĞ ĂƵƐĐƵůƚĂƟŽŶ ŵĞƚŚŽĚ͘ dŚŝƐ ŵĂŶƵĂů ĐŽŶƚĂŝŶƐ ŝŵƉŽƌƚĂŶƚ ƐĂĨĞƚLJ ĂŶĚ ĐĂƌĞ ŝŶĨŽƌŵĂƟŽŶ͕ ĂŶĚ ƉƌŽǀŝĚĞƐ ƐƚĞƉ ďLJ ƐƚĞƉ ŝŶƐƚƌƵĐƟŽŶƐ ĨŽƌ ƵƐŝŶŐ ƚŚŝƐ ďůŽŽĚ
INTRODUCTION CAUTION * This device is intended for adult use in homes only. * The device is not suitable for use on neonatal patients, pregnant women, patients with implanted, electronical devices, patients with pre-eclampsia, premature ventricular beats, atrial fibrillation, peripheral, arterial disease and patients undergoing intravascular therapy or arterio-venous shunt or people who received a mastectomy. Please consult your doctor prior to using the unit if you suffer from illnesses.
INTRODUCTION CAUTION * The service life of the cuff may vary by the frequency of washing, skin condition, and storage state. The typical service life is 10000 times. * It is recommended that the performance should be checked every 2 years and after maintenance and repair, by retesting at least the requirements in limits of the error of the cuff pressure indication and air leakage (testing at least at 50mmHg and 200mmHg).
INTRODUCTION BEFORE YOU START Monitor Components Component list of pressure measuring system h&& 1 Cuff 2 Air pipe 3 PCBA 4 Pump 5 Valve /Z ,K^ MEM O RY The Choice of Power Supply ϭ͘ ĂƩĞƌLJ ƉŽǁĞƌĞĚ ŵŽĚĞ͗ ϲs ϰп ďĂƩĞƌŝĞƐ Ϯ͘ ĂĚĂƉƚĞƌ ƉŽǁĞƌĞĚ ŵŽĚĞ͗ ϲs ϭ ;WůĞĂƐĞ ŽŶůLJ ƵƐĞ ƚŚĞ ƌĞĐŽŵŵĞŶĚĞĚ ĂĚĂƉƚĞƌͿ WůĞĂƐĞ ƵŶƉůƵŐ ƚŚĞ ĂĚĂƉƚĞƌ ƚŽ ĚĞƉĂƌƚ ĨƌŽŵ ƚŚĞ ƵƐŝŶŐ ƵƟůŝƚLJ ƉŽǁĞƌ͕ ǁŚĞŶ LJŽƵ ĮŶŝƐŚ ƚŚĞ ŵĞĂƐƵƌĞŵĞŶƚ͘ ME MO RY M S AC adaptor M /Z KEE dKZ W>h' WKt Z ^K < d S S TA R S TO
BEFORE BEFOREYOU YOUSTART START BEFORE BEFOREYOU YOUSTART START 4. ZĞƉĞĂƚ ƐƚĞƉƐ Ϯ ĂŶĚ ϯ ƚŽ ƐĞƚ ƚŚĞ DKEd, ĂŶĚ z͘ Setting Date and Time /ƚ ŝƐ ŝŵƉŽƌƚĂŶƚ ƚŽ ƐĞƚ ƚŚĞ ĂƚĞ ĂŶĚ dŝŵĞ ďĞĨŽƌĞ ƵƐŝŶŐ LJŽƵƌ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ŵŽŶŝƚŽƌ͕ ƐŽ ƚŚĂƚ Ă ƟŵĞ ƐƚĂŵƉ ĐĂŶ ďĞ ĂƐƐŝŐŶĞĚ ƚŽ ĞĂĐŚ ƌĞĐŽƌĚ ƚŚĂƚ ŝƐ ƐƚŽƌĞĚ ŝŶ ƚŚĞ ŵĞŵŽƌLJ͘ ;dŚĞ ƐĞƫŶŐ ƌĂŶŐĞ ŽĨ ƚŚĞ LJĞĂƌ͗ ϮϬϮϭͶϮϬϱϭ͕ dŝŵĞ ĨŽƌŵĂƚ͗ ϭϮͬϮϰ,Ϳ MEMORY MEMORY M M S S START START MEMORY 1.
MEASUREMENT BEFORE YOU START Tie the cuff 7. ZĞƉĞĂƚ ƐƚĞƉƐ Ϯ ĂŶĚ ϯ ƚŽ ƐĞƚ ƚŚĞ hE/d͘ MEMORY 1. ZĞŵŽǀĞ Ăůů ũĞǁĞůƌLJ͕ ƐƵĐŚ ĂƐ ǁĂƚĐŚĞƐ ĂŶĚ ďƌĂĐĞůĞƚƐ MEMORY ĨƌŽŵ LJŽƵƌ ůĞŌ Ăƌŵ͘ EŽƚĞ͗ /Ĩ LJŽƵƌ ĚŽĐƚŽƌ ŚĂƐ ĚŝĂŐŶŽƐĞĚ LJŽƵ ǁŝƚŚ ƉŽŽƌ ĐŝƌĐƵůĂƟŽŶ ŝŶ LJŽƵƌ ůĞŌ Ăƌŵ͕ ƵƐĞ LJŽƵƌ ƌŝŐŚƚ Ăƌŵ͘ 2. ZŽůů Žƌ ƉƵƐŚ ƵƉ LJŽƵƌ ƐůĞĞǀĞ ƚŽ ĞdžƉŽƐĞ ƚŚĞ ƐŬŝŶ͘ M M S S START START STOP TIME/DATE Pul/min STOP TIME/DATE Pul/min 8.
MEASUREMENT MEASUREMENT Start the Measurement ĞĨŽƌĞ LJŽƵ ƐƚĂƌƚ ƚŚĞ ŵĞĂƐƵƌĞŵĞŶƚ͕ ĚŽǁŶůŽĂĚ ƚŚĞ DĞĚD ,ĞĂůƚŚ ĂƉƉ ĨƌŽŵ WW ^ƚŽƌĞ Žƌ 'ŽŽŐůĞ WůĂLJ͕ ĂŶĚ ƚƵƌŶ ŽŶ ƚŚĞ ůƵĞƚŽŽƚŚ͘ /ŶƐƚĂůů ƚŚĞ WW͕ ĂŶĚ ƌĞŐŝƐƚĞƌ ĂŶ ĂĐĐŽƵŶƚ͘ dŚĞŶ ƐĞƚ LJŽƵƌ ƉĞƌƐŽŶĂů ŝŶĨŽƌŵĂƟŽŶ ;'ĞŶĚĞƌ͕ ŝƌƚŚĚĂLJ͕ ,ĞŝŐŚƚ͕ tĞŝŐŚƚ͕ EĂŵĞ ĂŶĚ ƐŽ ŽŶͿ͘ 1. ŝƐƉůĂLJ ƚŚĞ ůĂƚĞƐƚ ƌĞĐŽƌĚ͘ MEMORY ĚũƵƐƚ ƚŚĞ njĞƌŽ͘ Pul/min M M S S START START STOP STOP TIME/DATE Pul/min TIME/DATE Pul/min 2.
MEASUREMENT dŝƉ ϭ͗ ŶLJ ƟŵĞ ŝĨ LJŽƵ ǁĂŶƚ ƚŽ ƐƚŽƉ ƚŚĞ ŵĞĂƐƵƌĞŵĞŶƚ͕ ƉƌĞƐƐ ͞^d Zdͬ ^dKW͟ ďƵƩŽŶ͘ dŝƉ Ϯ͗ ŽƚŚ hƐĞƌ ĂŶĚ hƐĞƌ ĐĂŶ ƐƚŽƌĞ ŵĂdžŝŵƵŵ ϮϱϬ ŐƌŽƵƉƐ ŽĨ ƌĞĐŽƌĚ͘ tŚĞŶ LJŽƵ ƉĂƐƐ ƚŚĂƚ ůŝŵŝƚ͕ ĞǀĞƌLJ ƟŵĞ LJŽƵ ƚĂŬĞ ƚŚĞ ŵĞĂƐƵƌĞŵĞŶƚ͕ ƚŚĞ ŵŽŶŝƚŽƌ ǁŝůů ƉƌŽŵƉƚ ͞&h>>͟ ĮƌƐƚ ĂŶĚ ƚŚĞ ŽůĚĞƐƚ ƌĞĐŽƌĚ ǁŝůů ĚƌŽƉƐ ĨƌŽŵ ƚŚĞ ůŝƐƚ ĂŌĞƌ ƚŚĞ ŵĞĂƐƵƌĞŵĞŶƚ͘ >ŝƐƚ ŽĨ ĐŽŵƉĂƟďůĞ ĚĞǀŝĐĞƐ： &Žƌ ŝK^ ĚĞǀŝĐĞƐ͗ dŚĞ ŽƉĞƌĂƟŶŐ ƐLJƐƚĞŵ ŵƵƐƚ ďĞ ŝK^ ϭϯ͘Ϭ Žƌ ŵŽƌĞ͘ &Žƌ ŶĚƌŽŝĚ ĚĞǀŝĐĞƐ dŚĞ ŽƉĞƌĂƟŶŐ ƐLJƐƚĞŵ ŵƵƐƚ ďĞ ŶĚƌŽŝĚ ϱ͘Ϭ Žƌ ŵŽƌĞ CAUTION /ŶƚĞƌĨĞƌĞŶĐĞ
DATA MANAGEMENT INFORMATION FOR USER Delete the Records /Ĩ LJŽƵ ĚŝĚ ŶŽƚ ŐĞƚ ƚŚĞ ĐŽƌƌĞĐƚ ŵĞĂƐƵƌĞŵĞŶƚ͕ LJŽƵ ĐĂŶ ĚĞůĞƚĞ Ăůů ƌĞƐƵůƚƐ ĨŽƌ ƚŚĞ ƐĞůĞĐƚĞĚ ƵƐĞƌ ďLJ ĨŽůůŽǁŝŶŐ ƐƚĞƉƐ͘ ;dĂŬĞ hƐĞƌ ĨŽƌ ĞdžĂŵƉůĞ͘Ϳ 1. tŚĞŶ ƚŚĞ ŵŽŶŝƚŽƌ ŝƐ ŝŶ ƚŚĞ ŵĞŵŽƌLJ Tips for Measurement DĞĂƐƵƌĞŵĞŶƚƐ ŵĂLJ ďĞ ŝŶĂĐĐƵƌĂƚĞ ŝĨ ƚĂŬĞŶ ŝŶ ƚŚĞ ĨŽůůŽǁŝŶŐ ĐŝƌĐƵŵƐƚĂŶĐĞƐ͘ MEMORY ƌĞĐĂůů ŵŽĚĞ͕ ƉƌĞƐƐ ĂŶĚ ŚŽůĚ ͞^ d͟ ďƵƩŽŶ͕ ƚŚĞ > ǁŝůů ĚŝƐƉůĂLJ ͞Ě > >>͟ н hƐĞƌ / ͘ M S START STOP 2.
ABOUT BLOOD PRESSURE INFORMATION FOR USER What are systolic pressure and diastolic pressure? Maintenance /Ŷ ŽƌĚĞƌ ƚŽ ŐĞƚ ƚŚĞ ďĞƐƚ ƉĞƌĨŽƌŵĂŶĐĞ͕ ƉůĞĂƐĞ ĨŽůůŽǁ ƚŚĞ ŝŶƐƚƌƵĐƟŽŶƐ ďĞůŽǁ͘ ME MO ME MO RY tŚĞŶ ǀĞŶƚƌŝĐůĞƐ ĐŽŶƚƌĂĐƚ ĂŶĚ ƉƵŵƉ ďůŽŽĚ ŽƵƚ ŽĨ ƚŚĞ ŚĞĂƌƚ͕ ƚŚĞ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ƌĞĂĐŚĞƐ ŝƚƐ ŵĂdžŝŵƵŵ ǀĂůƵĞ ŝŶ ƚŚĞ ĐLJĐůĞ͕ ǁŚŝĐŚ ŝƐ ĐĂůůĞĚ ƐLJƐƚŽůŝĐ ƉƌĞƐƐƵƌĞ͘ tŚĞŶ ƚŚĞ ǀĞŶƚƌŝĐůĞƐ ƌĞůĂdž͕ ƚŚĞ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ƌĞĂĐŚĞƐ ŝƚƐ ŵŝŶŝŵƵŵ ǀĂůƵĞ ŝŶ ƚŚĞ ĐLJĐůĞ͕ ǁŚŝĐŚ ŝƐ ĐĂůůĞĚ ĚŝĂƐƚŽůŝĐ ƉƌĞƐƐƵƌĞ͘ Systolic Diastolic blood di
ABOUT BLOOD PRESSURE TROUBLE SHOOTING Why does my blood pressure fluctuate throughout the day? Why do I get different blood pressure at home compared to the hospital? dŚĞ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ŝƐ ĚŝīĞƌĞŶƚ ĞǀĞŶ ƚŚƌŽƵŐŚŽƵƚ ƚŚĞ ĚĂLJ ĚƵĞ ƚŽ ǁĞĂƚŚĞƌ͕ ĞŵŽƟŽŶ͕ ĞdžĞƌĐŝƐĞ ĞƚĐ͘ ůƐŽ͕ ƚŚĞƌĞ ŝƐ ƚŚĞ ͞ǁŚŝƚĞ ĐŽĂƚ͟ ĞīĞĐƚ͕ ǁŚŝĐŚ ŵĞĂŶƐ ďůŽŽĚ ƉƌĞƐƐƵƌĞ ƵƐƵĂůůLJ ŝŶĐƌĞĂƐĞƐ ŝŶ ĐůŝŶŝĐĂů ƐĞƫŶŐƐ͘ PROBLEM No power /Ĩ ƚŚĞ ĐƵī ŝƐ ƟĞĚ ƉƌŽƉĞƌůLJ͘ /Ĩ ƚŚĞ ĐƵī ŝƐ ƚŽŽ ƟŐŚƚ Žƌ ƚŽŽ ůŽŽƐĞ͘ /Ĩ ƚŚĞ ĐƵī ŝƐ ƟĞĚ ŽŶ ƚŚĞ ƵƉƉĞƌ Ăƌŵ͘ /Ĩ LJŽƵ ĨĞĞů ĂŶdžŝŽƵƐ
AUTHORIZED COMPONENT SPECIFICATIONS Power supply Display mode Measurement mode Measurement range Accuracy Normal working condition ĂƩĞƌLJ ƉŽǁĞƌĞĚ ŵŽĚĞ͗ ϲs ϰп ďĂƩĞƌŝĞƐ ĂĚĂƉƚĞƌ ƉŽǁĞƌĞĚ ŵŽĚĞ͗ ϲs ϭ ;WůĞĂƐĞ ŽŶůLJ ƵƐĞ ƚŚĞ ƌĞĐŽŵŵĞŶĚĞĚ ĂĚĂƉƚĞƌͿ͘ ŝŐŝƚĂů > s͘ ͘ ϲϬ ŵŵ п ϵϮ ŵŵ KƐĐŝůůŽŐƌĂƉŚŝĐ ƚĞƐƟŶŐ ŵŽĚĞ ZĂƚĞĚ ĐƵī ƉƌĞƐƐƵƌĞ͗ Ϭ ŵŵ,Ő Ε Ϯϵϵ ŵŵ,Ő ;Ϭ ŬWĂ Ε ϯϵ͘ϵ ŬWĂͿ DĞĂƐƵƌĞŵĞŶƚ ƉƌĞƐƐƵƌĞ͗ ^z^͗ ϲϬ ŵŵ,Ő Ε ϮϯϬ ŵŵ,Ő ;ϴ͘Ϭ ŬWĂ Ε ϯϬ͘ϳ ŬWĂͿ / ͗ ϰϬ ŵŵ,Ő Ε ϭϯϬ ŵŵ,Ő ;ϱ͘ϯ ŬWĂ Ε ϭϳ͘ϯ ŬWĂͿ WƵůƐĞ ǀĂůƵĞ͗ ;ϰϬͲϭ
FCC STATEMENT & ^ƚĂƚĞŵĞŶƚ & / ͗ KhϵdD ϭϰϵϬ , dŚŝƐ ĚĞǀŝĐĞ ĐŽŵƉůŝĞƐ ǁŝƚŚ WĂƌƚ ϭϱ ŽĨ ƚŚĞ & ZƵůĞƐ͘ KƉĞƌĂƟŽŶ ŝƐ ƐƵďũĞĐƚ ƚŽ ƚŚĞ ĨŽůůŽǁŝŶŐ ƚǁŽ ĐŽŶĚŝƟŽŶƐ͗ ;ϭͿ ƚŚŝƐ ĚĞǀŝĐĞ ŵĂLJ ŶŽƚ ĐĂƵƐĞ ŚĂƌŵĨƵů ŝŶƚĞƌĨĞƌĞŶĐĞ͕ ĂŶĚ ;ϮͿ ƚŚŝƐ ĚĞǀŝĐĞ ŵƵƐƚ ĂĐĐĞƉƚ ĂŶLJ ŝŶƚĞƌĨĞƌĞŶĐĞ ƌĞĐĞŝǀĞĚ͕ ŝŶĐůƵĚŝŶŐ ŝŶƚĞƌĨĞƌĞŶĐĞ ƚŚĂƚ ŵĂLJ ĐĂƵƐĞ ƵŶĚĞƐŝƌĞĚ ŽƉĞƌĂƟŽŶ͘ ĂƵƟŽŶ͗ dŚĞ ƵƐĞƌ ŝƐ ĐĂƵƟŽŶĞĚ ƚŚĂƚ ĐŚĂŶŐĞƐ Žƌ ŵŽĚŝĮĐĂƟŽŶƐ ŶŽƚ ĞdžƉƌĞƐƐůLJ ĂƉƉƌŽǀĞĚ ďLJ ƚŚĞ ƉĂƌƚLJ ƌĞƐƉŽŶƐŝďůĞ ĨŽƌ ĐŽŵƉůŝĂŶĐĞ ĐŽƵůĚ ǀŽŝĚ ƚŚĞ ƵƐĞƌΖƐ ĂƵƚŚŽƌŝƚLJ ƚŽ ŽƉĞƌĂƚĞ ƚŚĞ ĞƋƵŝƉŵĞŶƚ͘ EKd ͗ d
EMC GUIDANCE EMC GUIDANCE EMC Guidance Table 2 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.
EMC GUIDANCE Table 3 Guidance and manufacturer’s declaration - electromagnetic Immunity Radiated RF Test Band Service IEC61000-4-3 Frequency (MHz) (MHz) (Test specifications 385 380-390 TETRA for ENCLOSURE 400 PORT IMMUNITY to 450 430-470 GMRS 460, RF wireless FRS 460 communications 710 704-787 LTE Band equipment) 13, 745 17 780 810 870 930 1720 1845 1970 2450 5240 5500 5785 800-960 GSM 800/900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5 GSM 1800; 1700CDMA 1900; 1990 GSM 1900; DECT; LTE Band 1, 3, 4,2
