[DiaDENS-PC]
www.jpastar.com
This Operation Instructions (Ol) cover electrostimulator with built-in and remote electrodes, the portable one for stimulation
of the BAP and BAZ and for electropuncture diagnosis DiaDENS-PC.
The Operation Instructions includes Technical Passport and the Instructions for Operation proper.
PART 1. TECHNICAL PASSPORT
1. FUNCTION
The DiaDENS-PC device will be used for electric stimulation of biologically active points and zones (BAP and
BAZ), for auricular diagnosis, mini acupuncture diagnosis and the diagnosis by the Foil method. The device is
equipped with built-in and remote electrodes.
The DiaDENS-PC device is intended for individual application in therapeutic-prophylactic institutions and at
home in compliance with directions given by the attending physician, autonomously, or along with computer
diagnostics. The personal computer will be used for accumulation and storage of the diagnosis data.
2. TECHNICAL CHARACTERISTICS
2.1. Electric impulses of the device must have output parameters as follows:
2.1.1. the impulse minimal parameters:
- duration of the impulse positive part, us, not
exceeding
5
- amplitude of the impulse positive part, V, not
exceeding
10
- amplitude of the impulse negative part, V, not
exceeding
10
2.1.2.
maximal parameters of the impulse:
- duration of the impulse positive part, us, not
exceeding
500±70
- amplitude of the impulse positive part, V, not
exceeding
30±10
- amplitude of the impulse negative part, V, without
load
350±70
withload(20±5%)kOhm
300±70
2.2.
The device has the frequencies of impulse
sequence settings in Hz as follows:
2.2.1. Range 1:
- 10±2 including MED and SCREENING regimes
- 20± 2 - 6 0 ± 2 - 77± 2
- 77 Hz±2 and 10 Hz ± 2, modulated with frequency 2± 0.1 Hz
- 77 Hz± 2 with modulation by amplitude
- 140±5 - 200± 5
2.2.2. Range 2: from 1 to 9.9 with increment 0.1 ± 0.05.
2.3. The maximal used current (voltage 9 V.) not exceeding 40 mA.
2.4. Power supply:
battery of 6F22 type, voltage ............................................. 9 V
It will be admissible to use storage batteries of 6F22 type, voltage at least 9 B*.
2.5. Mass of the device, kg, not exceeding .....................0.35
2.6. With remote therapeutic and diagnostic electrodes, kg, not exceeding
0.7
2.7. Overall dimensions of the device, mm, not exceeding
210x55x45
2.8. Overall dimensions of therapeutic electrode, mm, not exceeding 125x10
2.9. Overall dimensions of passive diagnostic electrode, mm, not exceeding 100x20
Overall dimensions of active diagnostic electrode, mm, not exceeding
130x10
2.10. The device will be connected to the computer via serial port by protocol RS-232.
2.11. The device will be automatically switched off not later than in 10 minutes after the device has been idle
or after last application of electrodes to skin surface.
2.12. Operational conditions:
- surrounding temperature, °C......................................10-35
- relative air humidity at 25°C, not exceeding.....................93
If the device was stored at the temperature lower than 10°C,
keep it under normal climatic conditions for at least two hours prior to using it.
