Class IIa Medical Device

Automatic Noninvasive Health Screening Diagnostics

Based on the analysis of thermodynamic parameters — no needles, no blood draw, results in minutes.

139 Health Parameters
3–10 Minutes per Scan
0 Needles Required
Why ANESA

Key Features

A gentler, faster way to screen the essential markers of your health.

Noninvasive

Noninvasive Method

No blood sampling or other invasive procedures required

Fast

Fast Results

Examination takes only 3-10 minutes

Multiple Parameters

59 Health Parameters

Blood analysis, biochemical, hemodynamic and metabolic parameters

The Device

About the Device

Precision thermodynamic sensing packed into a compact, portable analyzer.

ANESA Device

Technical Specifications

  • Device Class IIa Active Medical Device
  • Measurement Accuracy ±0.1°C
  • Measurement Range +24 to +42°C
  • Examination Time 3-10 minutes
  • Parameters Measured 139 health parameters
  • Connection USB
  • Power Built-in rechargeable battery
Documentation

User Manual

Everything you need to operate the device safely and correctly.

General Information

1. General Information

The MD ANALYZER is a medical device for screening diagnostics of human health status based on analysis of thermodynamic parameters.

Safety Instructions

2. Safety Instructions

Important warnings and safety measures for proper device operation.

Measurement Procedure

3. Measurement Procedure

Step-by-step guide for conducting examinations.

We're Here to Help

Support

Reach out with any question about the device, software or documentation.

Contact

Contact Information

Manufacturer: X0-Soft LLC
Address: Georgia, Tbilisi 0179, lia Chavchavadze av., 1-st deadend 4, apt.6
Phone: +44 7366 322104 (WhatsApp)
Email: anesahealth@gmail.com
Website: www.anesa.biz

Frequently Asked Questions

The device should not be used in pediatrics, critical/urgent states, ICU departments, for patients undergoing chemotherapy or X-Ray therapy, or patients with diabetes mellitus, jaundice, acute kidney insufficiency. Also contraindicated for donors after blood transfusion (6 months) and recipients after blood transfusion.

The device measures temperature with accuracy not less than 0.07°C. A number of parameters determined by the analyzer were tested during several clinical trials where their reliability has been confirmed.

Get Started

Downloads

Software, apps and documentation to get your device up and running.

Software

Software

USPIH software version 9.7X and higher

Download
Android App

Software

Android App

Download
Documentation

Documentation

Complete technical documentation

Download
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