Electronic equipment for medical technology - Import export

OB2012 medical suction unit equipped with: OB-J collection jar for 1000 ml SERRES® disposable bags recharging cable complete with cigarette lighter plug and two-pole connector Nominal suction power: 800 mbar (80 kPa) ±10% Nominal suction flow: 30 LPM at free air speed ±10% Maximum operating time (free-cycle): 60 minutes ±10% Degree of protection against infiltration of liquids and solids: IP34d Functioning/charge: 12÷15 Vdc Maintenance-free piston pump Sealed lead-acid battery The suction unit can be equipped with an OB WB charging bracket (in accordance with EN 1789) and an external mains-voltage power supply with two-pole plug (mains power supply between 100 and 240 Vac) Dimensions: 350x240x120 mm Weight: 4.6 kg complete with accessories, without support bracket Class IIa medical device in compliance with Regulation (EU) 2017/745 (MDR), all applicable regulations and main reference standards

OB500 medical suction unit equipped with OB-J collection jar for 1000 ml SERRES® disposable bags The device is designed for medical vehicles and is stationary, not portable Nominal suction power: 800 mbar (80 kPa) ±10% Nominal suction flow: 30 LPM at free air speed ±10% Maximum operating time (free-cycle): 60 minutes ±10% Degree of protection against infiltration of liquids and solids: IP32d Functioning: 12÷15 Vdc Maintenance-free piston pump Vacuum control and regulation unit to be embedded on the wall Dimensions of suction unit: 175x175x100 mm Dimensions of standard built-in adjustment unit: 53x110x70 mm Weight: max. 2 kg including mounting parts Class IIa medical device in compliance with Regulation (EU) 2017/745 (MDR), all applicable regulations and main reference standards

Carries out spectrophotometric analysis with the registration of arterial temperatures infrared radiation. Cannot be used without an interface block. The module can: • noninvasively obtain 85 biochemical parameters of peripheral and hemodynamic blood composition; • obtain hemodynamic parameters; • obtain various information about the oxygen transportation in the blood; • analyze the cardiovascular system activity; • study affiliation with the hematopoietic, immune and enzyme systems of the body.

The robotic wheelchair with the function of verticalization developed by JSC “SPA “Android Technics” and manufactured by JSC “IC SPA “Android Technics”. Features: 1. Flexible settings in accordance with a disease for the physiology of each patient weighing up to 140 kg. 2. Autonomous movement independently from other persons. Power reserve on a single charge is up to 35 km with an average speed of 6 km/h. 3. Electric footrest lowered to the floor may be used for any length of your legs. 4. Excellent maneuverability in small spaces combined with exceptional stability. The verticalization accelerates the rehabilitation process after a long stay in the supine and sitting positions. Delivery set: 1 Basic (without verticalization system). 2 Standard (with verticalization system). Warranty period: 12 months.

The robotic complex Orthosis-1 for treatment patients through the "brain-computer" interface. It is recommended for post stroke patients, patients with posttraumatic hand and legs palsy of any intensity and limitation, and children with cerebral palsy. Features: 1. Provides grasping and disclosure of the human relaxed hand due to the commands sent by an operator through the interface of a specialized software. 2. Rehabilitation procedure involves stimulation of brain neuroplasticity mechanisms, activated by the imagination of movements. 3. The technology is based on fundamental research of brain neuroplasticity and tested in multicenter blind randomized clinical research on more than 100 patients. Warranty period: 12 months.

Sensitiv imago® 530 is the previous model in the SensitivE line. Hi-tech hardware-software complexes for diagnostic scan, analysis and healing of organism. Senstiv imago 530 device is being assembled according to the new European quality management standards 9001 full accepted in EU in 2013. The device passed the medical laboratory testing class 2, according to the European Directive.

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