Because these devices may come into contact with perioral skin, saliva, and other biological materials during a choking emergency, their safety and reusability must be supported by rigorous scientific validation.
To support responsible emergency preparedness, Fitiger conducts independent third-party laboratory testing to evaluate the safety, cleaning procedures, disinfection effectiveness, and usability of its airway rescue devices.
Testing programs follow internationally recognized evaluation approaches commonly used for non-invasive medical and emergency response devices, including laboratory validation, worst-case contamination scenarios, and usability evaluation.
Available documentation may include laboratory validation summaries, testing protocols, and technical white papers supporting Fitiger airway rescue technology.
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