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SECTION 2
Nexalin ADI Device Specifications
The Nexalin ADI Device, its components, and all accessories are latex-free.
Applicable Standards
The Nexalin ADI Device complies with the following standards:
AAMI/ANSI SW68
IEC 60601-1, IEC 60601-1-2
CAN/CSA C22.2 No. 601.1-1-M90
IEC 60601-1-4
ISTM 2A
UL 60601-1
Note: This equipment has been tested and found to comply with the EMC limits for MDD 93/42/EEC
(EN 55011 Class B and EN 60601-1-2). These limits are designed to provide reasonable protection
against harmful interference in a typical medical installation. The equipment generates, uses, and can
radiate radio frequency energy. If not installed and used in accordance with these instructions, it may
cause harmful interference to other devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation.
Electrical
Nexalin ADI Device power source: 100-240 V~, 50/60Hz, 0.6A.
Fuses: Two 5 x 20 mm Slo-Blo 1.0A, 250V, double-pole/neutral.
Power cord rating: 250V AC, 10A, 3 wire, 18AWG, Type SJT, grounding type,
IEC 60320-C13, NEMA 5-15P hospital-grade plug cap, 3m (~9ft) long, UL and CSA approved. Only cords with the
above rating assure grounding reliability when connected to the equivalent receptacle.
Waveform: Modulated 100 kHz stimulation with the waveform current and treatment duration preset by the
manufacturer.
Environmental
Operational:
41°F (5°C) to 104°F (40°C) and out of direct sunlight
Relative humidity (RH) range of 5% to 90%
Transport and Storage:
-4°F (-20°C) to 131°F (55°C)
Relative humidity (RH) range of 5% to 90%
Atmospheric pressure: 7.25psi to 15.37psi (50kPa to 106kPa)
Electrodes: temperature-controlled environment and out of direct sunlight
Mechanical
Dimensions: Width 10in (25.4cm) x Height 4.5in (11.4cm) x Depth 10.5in (26.7cm)
Weight: 6lb (2.72kg)