Braun ExactFit 3 BP 6000 Anleitung Seite 7

Specifications
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.
Inflation 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.
Unit weight Approximately 500gr (without batteries)
Power supply Alkaline battery: 4 x AA (LR6)
Battery life 300 times measurement
Auto power off Whenever not used for 1 minute
Accessories 4 batteries, 2 arm cuffs with tube, instruction manual, pouch,
travel bag
IMPORTANT
Read the operating instructions.
Classification:
• Internally powered equipment
• Type B equipment
• IP22
• Not suitable for use in the presence of flammable anesthetic mixture with air, oxygen
or nitrous oxide
• Continuous operation with short-time loading
Operating temperature
Storage temperature
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This product conforms to the provisions of the EC directive 93/42/EEC (Medical Device
Directive). This device conforms to the following standards:
0297
• 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
package insert).
Portable and mobile RF communications equipment can affect 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
See warranty statement inside the Guarantee/Consumer Card/Authorized Service Centers booklet.
If for any reason you have to return your device to the point of sales or authorized Service Center,
please fully complete the Consumer Card (provided with the device) and insert it inside of the box
before you return your device.
The Consumer Card can also be found in Kaz Europe website (www.hot-europe.com/customer-care/
repair-services/) and you can download it in the case that you lose the one provided with the device.
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 affects your rights under statutory law.
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