Michigan Instruments’ CPR product line offerings are registered as “Class II” medical devices by the U.S. Food and Drug Administration (FDA) per the Code of Federal Regulations, (21 CFR820). Additionally, Michigan Instruments complies with FDA Quality System Regulation (QSR) requirements cited in (21 CFR820).

Michigan Instruments maintains a Quality Management System (QMS) compliant to ISO 13485:2016.

Download a .pdf version of the certificate here, if desired.

For more information on the certifying authority, click here.

Michigan Instruments, Inc. Videos

Michigan Instruments Lung Simulator Software, PneuView Overview - Video

The PneuView3 Training and Test Lung System - Video

How To Set Up A Simulation Of Spontaneous Breathing Adult Patient Using Dual Adult Lung Simulators - Video

Breathe Even Easier: The Spontaneous Breathing Lung (SBL) is Here - Video

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