• Power supply: - Internal 4.5 V, with 3 alkaline 1 5V AAA batteries (LR03).
• Battery life: 20 hours / 40 sessions with standard alkaline batteries (varies
depending on the program and stimulation level).
• Electrical safety class: Internally powered according to IEC
60601-1.
• Operating mode: continuous.
• Usage time: Based on the selected program; the device
has no usage-time restrictions and can be used
continuously (until the primary batteries are fully discharged).
• Stimulation output intensity: from 1 to 99 mApp in 1 mA steps on
a 1 kΩ load (with 200 μs pulses);
• Programs: 5 preset for quick use (PRESET).
• Output waveform: fixed; P1 - P4 alternating symmetrical biphasic
pulses; P5 symmetrical biphasic pulses.
• Energy: - approximately 2 mJ for each pair of pulses.
• DC component at output: max. 4 mVrms
• WORK time: Preset according to the selected program: from
3 to 60 seconds (±0.5 seconds) or Continuous.
• REST time: Preset according to the selected program: from
1 to 7 seconds (± 0.5 seconds).
• Session duration: From 15 to 50 minutes (± 0.5 minutes), depending on the program.
• Patient circuit output connection: 1 channel via a connector
micro-coaxial, to which the cable with 2 ends fitted with
a plug protected by 2 mm (patient side) is connected.
• Applied part: Perineal probe or surface electrodes. •
• Electrode circuit monitoring: stimulation intensity is reset to zero if the
electrode connection is interrupted or if the electrodes do not adhere
sufficiently to the skin.
• Frequency: Preset according to the selected program: 1 to 100
Hz (± 5%).
• Frequency during Rest: Preset according to the selected
program: from 3 to 10 Hz (± 5%).
• Pulse width – fixed according to the selected program: from 50 to
300 us (± 5%).
• Electromagnetic susceptibility: Complies with Class A according to
CISPR 11.
• Dimensions: - 90x50x30 mm. Weight: - approx. 90 g (including batteries).
• Operating and storage environment: Operating +5°C/+40°C (15% / 90%
RH - 700 hPa / 1060 hPa) - Storage -25°C / +70°C - (90% RH)
• Protection against ingress of solids and liquids: IP22
• CE marking: Class IIa device according to Rule 9, Annex
VIII 2017/745 MDR - CE0051 marking, issued by IMQ,
according to Annex IX of Regulation 2017/745.
• Production quality control: certified under the ISO9001 - ISO13485
system.
• CND - EMDN: Z12062701

• 1 miniSTIM electronic stimulator;
• 1 vaginal probe;
• 1 pack of 4 reusable electrodes, 50x50 mm;
• 1 cable for connecting miniSTIM to the supplied vaginal probe;
• 1 cable for connecting miniSTIM to the surface electrodes;
• 3 LR03 alkaline batteries (AAA);
• 1 storage bag;
• 1 miniSTIM user guide;
• 1 miniSTIM quick guide.