10. Technical speciications
Cuf pressure
Cuf size
Timing time
Voltage supply for battery operation
Permissible operating conditions
Permissible storage conditions
Permissible transport conditions
Dimensions
Total weight
Protection class
Classiication
The serial number is located on the device or in the battery compartment.
11. Mains part
Voltage supply for mains operation
Polarity
Protection class
Executive standards
This product conforms to the following standards and regulations
• EN 60601-1: 2006 + A1: 2013 Medical electrical equipment — Part 1: General requirements for basic safety and
essential performance
• EN 60601-1-11: 2010 Medical electrical equipment General requirements for basic safety and essential perfor-
mance- Collateral standard: Requirements for medical electrical equipment and medical electrical systems used
in the home healthcare environment
• EN 60601-1-2: 2015 Medical electrical equipment — Part 1-2: General requirements for safety — Collateral
standard: Electrom agnetic compatibility — Requirements and tests
max. 120 mmHg (when correctly used, as described in
section 7.1.)
29 – 53 cm
10 – 30 minutes with a deviation of ± 10 %
6 V DC (4 x 1.5 V
+5 °C to +40 °C, 15-93 % relative humidity (non-conden-
sing), 700 hPa – 1060 hPa ambient pressure.
-25 °C to +70 °C, 0 – 93 % relative humidity (non-conden-
sing), 700 – 1060 hPa ambient pressure.
-10 °C to +40 °C, 15 – 93 % relative humidity (non-con-
densing), 700 – 1060 hPa ambient pressure.
Leg cuf: 61 x 67 x 0.5 cm
Hand switch: 17 x 7.7 x 3 cm
approx. 1400 g (without mains part)
Type BF
Input: 100–240 V~ 50/60 Hz, 200 mA
Output: 6 V DC, 500mA
22
AA batteries (alkaline type LR06))