Braun ExactFit 3 Mode D'emploi page 7

Specifi cations
Method of measurement Oscillometric
Model number BP6000, BP6100, BP6200
Range of measurement Pressure 0~300 mmHg
Pulse 40~199 beats/minute
Accuracy Pressure +/- 3 mmHg
Pulse +/- 5 % Max.
Infl ation Deluxe automatic
Display Liquid crystal display – systolic, diastolic, pulse rate
Backlight Display for BP6200
Sets of memory BP6000: 40 sets per user
BP6100: 50 sets per user
BP6200: 60 sets per user
Cuff size Small cuff = 22-32cm arm circumference
Large cuff = 32-42cm arm circumference
Operating temperature +10 °C ~ + 40 °C, less than 85 % R.H.
Storage temperature -20 °C ~ +60 °C, less than 85 % R.H.
Operating atmospheric pressure 860-1060 hPa
Unit weight Approximately 500gr (without batteries)
Power supply Alkaline battery: 4 x AA (LR6) 1.5V
Battery life 300 times measurement
Auto power off Whenever not used for 1 minute
Accessories 4 batteries, 2 arm cuff s with tube, instruction manual, pouch,
travel bag
Service life: 5 years.
IMPORTANT
Read the operating instructions.
If device is not used within specifi ed temperature, humidity and atmospheric pressure
ranges, the technical accuracy of the measurement cannot be guaranteed.
Classifi cation:
• Internally powered equipment
• Type BF equipment
• IP22: Protected against solid foreign objects of 12.5 mm diameter and greater.
Protected against vertically falling water drops when the device is tilted up to 15°
• Not suitable for use in the presence of fl ammable anesthetic mixture with air, oxygen
or nitrous oxide
• Continuous operation with short-time loading
Operating temperature
Storage temperature
Subject to change without notice.
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All manuals and user guides at all-guides.com
Storage humidity
This product conforms to the provisions of the EC directive 93/42/EEC (Medical Device
Directive). This device conforms to the following standards:
• EN 60601-1: 2006 + AC:2010: - General requirements for basic safety and essential
performance
• EN 60601-1-2:2007 - Electromagnetic compatibility requirements and tests
• EN 60601-1-11:2010 - Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment
• EN 1060-1:1995 + A2:2009 – Non-invasive sphygmomanometers - general
requirements
• EN 1060-3:1997 + A2:2009 - Non-invasive sphygmomanometers - Supplementary
requirements for electro-mechanical blood pressure measuring systems.
• EN 1060-4:2004 - Non-invasive sphygmomanometers - Test procedures to determine
the overall system accuracy of automated non-invasive sphygmomanometers.
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For detailed description of EMC requirements please contact an authorized local Service Centre (see
guarantee).
Portable and mobile RF communications equipment can aff ect medical electrical equipment.
Please do not dispose of the product in the household waste at the end of its useful life.
Disposal can take place at your local retailer or at appropriate collection points provided
in your country.
Guarantee
Consumer Card available on our website at www.hot-europe.com/after-sales
Please see last page of this manual to fi nd the contact for the Kaz Authorized Service Center in your
country.
The LOT and SN of your device are printed on the rating label in the back of the product.
UK only:
This guarantee in no way aff ects your rights under statutory law.
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