Braun iCheck 7 BPW 4500 Manual De Instrucciones página 7

Specifications
Model BPW4500
Measurement method Oscillometric
Display OLED display
Blood pressure measurement range 40 ~ 255mmHg
Pulse measurement range 40 ~ 199 beats/minute
Calibration accuracy Blood pressure: +/- 3 mmHg
Pulse rate: +/- 4% of reading
Inflation/Deflation Automatic
Sets of memory Up to 100 readings
Cuff size Fits wrist circumference: 12.5 - 21 cm (4.9 - 8.3 inch) min/max
Operating temperature +10 °C ~ + 40 °C, less than 85 % R.H. non-condensing
Storage temperature -20 °C ~ +55 °C, less than 85 % R.H. non-condensing
Unit weight Approximately 125g (exluding batteries)
Power source Alkaline battery: 2 x AAA (LR3) 1.5V
Auto power off Approx. 60 seconds
Service life 5 years
Wireless communication Bluetooth® Smart
Frequency Range: 2.4GHz ISM Band (2400 - 2483.5 MHz)
Modulation: GFSK
Effective radiated power: <20dBm
Important
Read the operating instructions.
If the device is not used within the specified temperature, humidity and atmospheric pressure ranges,
the technical accuracy of the measurement cannot be guaranteed.
Classification:
Internally powered equipment
Type BF applied parts
Protected against solid foreign objects of 12.5 mm diameter and larger. Protected against water drops falling
vertically when the device is tilted up to 15°.
Not suitable for use in the presence of flammable anaesthetic mixtures with air, oxygen or nitrous oxide.
Continuous operation with short-time loading.
+40°C
+55°C
Operating temperature Storage temperature
+10°C
-20°C
10
Storage humidity
Subject to change without notice.
This device conforms to the following standards:
EN 60601-1:2006/A1:2013 - General requirements for basic safety and essential performance.
EN 60601-1-2:2015 - Medical Electrical Equipment - Electromagnetic compatibility - Requirements and tests.
EN 60601-1-11:2010 - Medical Electrical Equipment - Requirements for medical electrical equipment and medical electrical
systems used in the home healthcare environment.
EN 1060-3:1997 + A2:2009 - Non-invasive sphygmomanometers - Supplementary requirements for electromechanical blood
pressure measuring systems.
EN 1060-4:2004 - Non-invasive sphygmomanometers - Test procedures to determine the overall system accuracy of
automated non-invasive sphygmomanometers.
This product conforms to the provisions of the EC Directive 93/42/EEC (Medical Device Directive and
superseding regulations).
This product carries the CE mark and is manufactured in conformity with the RoHS Directive 2011/65/EU.
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For a detailed description of EMC requirements please contact an authorised local Service Centre (see guarantee) or visit
www.hot-europe.com/support.
Portable and mobile RF communications equipment can affect medical electrical equipment.
This product contains batteries and recyclable electronic waste. To protect the environment, do not dispose
of it in household waste, but take it to an appropriate local collection centre provided in your country.
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