Our last innovations are Smart one and Smart one oxi: the first app-based personal Spirometers (PEF,FEV1), with or without embedded Oximeter (SpO2, Pulse), now available on your SmartPhone and Tablet, via Bluetooth Smart 4.0.

A step forward in health care management.


MIR healthcare solutions are CE marked and approved by the FDA*.
The FDA (Food and Drug Administration), is the U.S. government agency in charge of regulating food and pharmaceutical products, dependent on the U.S. Department of Health and Human Services.
The FDA's purpose is the protection and preservation of the public's health by ensuring the products under its jurisdiction are safe, wholesome, sanitary and properly labeled.
FDA registration is subject to review every two years as a prerequisite for exporting specific product categories that are under the FDA's jurisdiction to the US market. With FDA registration and numerous other certifications, MIR product compliance has made its device available in over 100 countries, with more becoming available regularly.
MIR is internationally recognized for the uniqueness of our patented products.

International Patent granted for the Design of Smart One and Smart One Oxi.

*Waiting for Smart One Oxi
  • American Thoracic Society
  • European Respiratory Society
  • ISO 26782 for Spirometry
  • ISO 23747 for Peak Flow
  • ISO 80601-2-61 for Oximetry