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System for diagnostics of motor pathology and rehabilitation treatment by biofeedback method "Stadis" (II.

Functional Diagnostic Devices

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Key Highlights

Made in Russia - engineered for durability
Suitable for challenging environments
Lower cost of ownership than European alternatives
Bulk orders available with volume discounts
Documentation and customs clearance assistance provided

Available Models

System for diagnostics of motor pathology and rehabilitation treatment by biofeedback method "Stadis" (I. System for diagnostics of motor pathology and rehabilitation treatment by biofeedback method "Stadis" (III).

Description

The specialised biofeedback simulator "Stadis" allows assessment of walking parameters and rehabilitation based on the results of the examination. The Stadis simulator uses Neurosens biometric sensors to record walking parameters. These miniature devices are mounted on the patient's shins (and/or back) and record rotational velocities and accelerations in three axes, as well as electromyograms in two channels. Up to 20 walking parameters can be recorded in total. The sensors are wireless, battery-powered and transmit data to the software via Wi-Fi. They are not affected by nearby metal structures. The Gait Analysis Lab is a professional system for objective assessment of walking function. It analyses walking function in more than 25 different parameters, including joint angles. Up to 12 inertial sensors can be used simultaneously.

Specifications

Appointment of the device 1) analysis of biomechanical/neuromuscular function of walking, postural studies and joint mobility using specialised equipment; 2) neuromuscular rehabilitation therapy of different anatomical areas based on mutual

Method of motion registration Biometric sensors

Automatic calculation of walking time parameters, walking phases, spatial parameters of walking, kinematic parameters of walking availability

Video recording of evaluation procedures availability

Automatic generation of evaluation and training protocol availability

Saving completed assessments and drills, as well as their protocols in the database availability

Ability to change the list of calculation parameters for biomechanical/neuromuscular function and postural function analyses availability

Ability to view previously completed assessments/exercises of walking function, balance and body balance, coordination, and d availability

Ability to create custom protocol templates for assessment and training of walking, balance and t-balance function availability

Built-in protocol template editor availability

Ability to edit evaluation and training protocols availability

Ability to include graphs, figures and tables in the protocols availability

Availability of a consolidated protocol to track the dynamics of rehabilitation availability

Base of medical norms on basic parameters of walking (phases of walking, temporal parameters, spatial parameters, kinematics) availability

Monitoring the condition of equipment during evaluations and drills availability

Types of registration channels accelerometric, gyroscopic, electromyographic

Sensor weight Not more than 40 (± 4) g

Dimensions of the sensor Not more than 60×40×17 (± 2) mm

Wireless communication with PC availability

communication range Not less than 10 metres in line of sight

Maximum number of sensors simultaneously linked to one PC Not less than 12 pcs.

Sensor synchronization accuracy max. 0.005 s discrepancy

Quantization frequency at least 200 Hz

Input range of measured accelerations in each of the three axes At least ±16g

Permissible error of acceleration measurement in each of the three axes not more than ±(0.04 g + 5% of the measured value)

Input range of angular velocities in each of the three axes Not less than ± 2000 deg/sec.

Permissible error of angular velocity measurement in each of the three axes not more than ±(0.5 deg/s + 2% of measured value)

Total number of differential channels per 1 sensor At least 2

Quantization frequency at least 2 kHz

In-phase noise reduction (CMRR) At least 100 dB

Lower bandwidth limit at level (-3 ± 0.5) dB in EMG measurement mode max. 5 Hz

Upper limit of the bandwidth at the level of (-3 ± 0.5) dB in the EMG measurement mode at least 500 Hz

Natural noise level in EMG measurement mode Not more than 2 µV RMS

Input differential resistance At least 100 megohms

EMG signal input range max. 0.07 µV - 20 mV

EMG signal measurement error in the input range from 0.07 µV to 20 mV and at the bandwidth from 5 to 500 Hz not more than ±(7 ?V + 5% of the measured value)

Suppression of mains interference by a switchable tap selector filter At least 40 dB

Function for determining the sub-electrode impedance availability

Note: All specifications are provided by the manufacturer and may be subject to change. Please contact us to confirm the latest specifications before placing your order.

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Shipping Terms

FOB Novorossiysk, Russia CIF Available to major ports worldwide EXW Manufacturer's facility, Russia

Delivery Time

Sea freight: 30-60 days (depending on destination) Air freight: 14-21 days (for urgent orders)

Payment Methods

Letter of Credit (L/C) Wire Transfer (T/T) Escrow Services

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