Important - Braun ActivScan 9 Mode D'emploi

Specifications
Model number BUA7200
Method of measurement Oscillometric
Blood pressure measurement range 40 ~ 255 mmHg
Pulse measurement range 40 ~ 199 beats/minute
Calibration accuracy Blood pressure: +/- 3 mmHg
Pulse rate: +/- 4% of reading
Inflation/Deflation Automatic
Display Color TFT dot matrix display
Sets of memory Up to 200 readings per user
Cuff size Universal cuff: 22-42 cm (9-17 inch) min/max arm
circumference
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 610g (excluding batteries)
Power source Alkaline battery: 4 x AA (LR6) 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
Operating temperature
10 °C
Storage humidity
Subject to change without notice.
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Storage temperature
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.
This product conforms to the provisions of the EC Directive 93/42/EEC
(Medical Device Directive).
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.
Hereby, Kaz Europe Sàrl, declares that the radio equipment type BUA7200 is in compliance with
Directive 2014/53/EU. The full text of the EU declaration of conformity is available at the following
internet address www.hot-europe.com/support.
This product contains batteries and recyclable electronic waste. To protect the
environment, do not dispose of it in household waste, but take it to appropriate local
collection centre.
English
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