產品說明 Product description 產品說明 Start BP 6200 This product is manufactured by Kaz Europe Sàrl under a license to the ‘Braun’ trademark. ‘Braun’ is a registered trademark of Braun GmbH, Kronberg, Germany. 此產品由歐洲卡舒公司( )以百靈牌商標認可生產, 德國百靈公司 Kaz Europe Sàrl Braun GmbH, Kronberg, Germany )為百靈牌商標持有人。...
Intended use of Braun ExactFit 5 • This product is intended for household use only. Keep product and batteries away from Braun upper arm blood pressure monitor has been developed for accurate and comfortable blood children. pressure measurements. The measuring accuracy of Braun’s upper arm blood pressure monitor was • People suffering from cardiac arrhythmia, vascular constriction, arteriosclerosis in...
• Do not in any way twist the arm cuff. Display BP6200 • Do not inflate the monitor’s cuff when it is not wrapped around the arm. • Do not attempt to disassemble or change any parts of the monitor including the cuff. • Do not drop the product or put it through strong impact.
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Select mode 6. LCD Display will show the results and WHO indicator arrow after measurement. After taking blood pressure measurement, turn off the device by pressing the start button (1) or How to select user A /user B automatically after 1 minute. • Make sure the Product is in power off mode.
What to do if ….. Irregular heart beat detector Problem Reason Solution The appearance of this symbol signifies that a certain pulse irregularity was detected during the Heart rate Appears in the measurement • Measurement in progress, remain quiet. measurement. Talking, moving, shaking or an irregular pulse during the measurement can result in the symbol condition and flashes when appearance of this icon.
The warranty becomes void • Type BF equipment if repairs are undertaken by unauthorized persons and if original Braun parts are not used. To obtain • IP22: Protected against solid foreign objects of 12.5 mm diameter and greater.
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Guidance and manufacturer’s declaration – electromagnetic immunity Guidance and manufacturer’s declaration – electromagnetic emissions The ME is intended for use in the electromagnetic environment specified below. The ME equipment is intended for use in the electromagnetic environment specified below. The customer or the user of the ME should assure that it is used in such an environment. The customer or the user of the ME equipment should assure that it is used in such an environment.
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規格 本產品符合EC指引93/42/EEC的規定(醫療器械指引),並符合以下標準: 量度模式 示波測定法 • E N 60601-1: 2006 + AC:2010: - General requirements for basic safety and essential 型號 BP 6200 0297 performance 量度範圍 壓力0~300 mmHg(毫米汞柱) • EN 60601-1-2:2007 - Electromagnetic compatibility requirements and tests 脈搏40-199次/分鐘 • EN 60601-1-11:2010 - Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment 精確度 壓力+/-3 mmHg(毫米汞柱) • EN 1060-1:1995 + A2:2009 – Non-invasive sphygmomanometers - general 脈搏+/- 5%(最多) requirements 充氣 自動 • EN 1060-3:1997 + A2:2009 - Non-invasive sphygmomanometers - Supplementary requirements for electro-mechanical blood pressure measuring systems.