EIS Scan.com

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Electro Interstitial Scan

Less Time, More Accurate, Greater Results!

Proven
Time tested by European medical professionals for more than ten years.

The EIS offers today’s health practitioners an unparalleled, non-invasive assessment of their client’s physiology.

Speed
In just three minutes, a complete analysis is presented of your client’s top risks.

Before and After Treatment Scans
Is your intervention and care making a difference that your client can see?
Improve patient compliance and enhance their mind-body connection an bring the effectiveness of your treatment home.

The EIS System (a.k.a. "EIS"; Electro Interstitial Scan-BF):

Type of device The EIS is a programmable electro medical system (PEMS) including:

USB plug and play hardware devices including interface devices, disposable electrodes, reusable plates and reusable cables.

Software installed on a computer.

The EIS v.10 is classified as bioimpedance device . The signal processing analysis displays the parameters of the living tissue related to the electrical conductivity and electrical dispersion.

The device is using the Bioimpedance technology in bipolar mode with a very low frequency.

Indications or Intended use

According to the clinical investigations::

The EIS is intended for use as adjunct in follow ups of drugs’ administration (thyroid hormone, beta blockers, ACE inhibitors and SSRI treatments)and ADHD children diagnosis with the conventional methods.

The EIS is designed to be used with children (over 5 years) and adult patients.

The device is not intended for use in support life and not for continuously monitoring. The system should be used by a certified practitioner.

ES Teck PEMS

ES TECK PEMS

EC marks (Class IIa) , Health Canada (Class III) , and FDA 510k Clearance >Description of the features The ES Teck System is a programmable electro medical system (PEMS) including: •USB plug and play hardware device including an electronic box , 3 disposable electrodes, reusable Adult SpO2 probe and reusable cables •Software installed on a computer. E.S Teck system is a combination of 2 devices (or modules) with specific features controlled by unique software: - Pulse Oximeter displays SpO2%, pulse rate value and vertical bar graph pulse amplitude. The photoelectrical Plethysmograph’ feature (PP) analyzes the pulse waveform provided by the oximeter. - HRV (Heart Rate Variability) evaluates the variation of the heart rate, both in the time domain (statistical methods) and in the frequency domain (spectral analysis). Each QRS complex is detected and the so-called normal-to-normal (NN) or Rate-to-Rate (RR) intervals between adjacent QRS complexes are resulting from sinus node depolarization. >Indications / Intended uses Each module has specific feature and intended use 1.Pulse Oximeter: •To spot check or monitor Oxygen saturation of arterial hemoglobin (SpO2%) and pulse rate. •To analyze the pulse waveform (Photoelectrical Plethysmography or PP) provided by the oximeter. It only provides mathematical analyses of the input of the SpO2. 2.Heart rate variability (HRV) : •To analyze the basic rhythms of the NN or RR intervals in heart rate, both in the time domain and in the frequency domain (short time 5 minutes). It only provides mathematical analyses of the input of the heart rate variability. The mathematical analysis of Photoelectrical Plethysmography and HRV are not intended use for diagnosis. The software provides a visual alarm for the values of the heart rate and/or SpO2 percent out of the normal range and for the bad quality signal transmission. The data are stored in PC in the Backup system of the ES Teck software. The device is intended use only for adult subjects (> 20 years old) This Oximeter is intended to be used in spot-checking (2 minutes) The device is intended use in licensed practitioner’s office This device is no intended to be used at home, in hospital or out-of-hospital transport The device is not intended use in support life and not for continuously monitoring The system will be used by licensed practitioner.

Certificates

ISO 13485 : 2003. No. 2114028 Kema Medical
Health Canada Class II & Class III Medical Device
CE 0344 Class II a Kema Medical
U.S. patent Number. US 61/194,509

For a consultation or free demonstration to learn more about how much the EIS can contribute to your bottom line, please contact us.

Multi-Discipline Support