Altair Medical’s RESPMETER^TM is a chest-worn wireless sensor that accurately detects when someone is suffering Opioid Indused Respiratory Depression (OIRD), a common and often fatal side effect of using opioid drugs. Causing 1,000 deaths each week in the UK and USA, OIRD is now the largest cause of accidental death in most developed countries.

The technology monitors and analyses respiratory patterns using proprietary algorithms. When it detects OIRD in the patient, it sends a message to designated first responders, or emergency services, who can intervene to administer naloxone. This extemely effective antidote has a very high success rate, reviving the person within seconds.

The Breakthrough Devices Program was established by the FDA to provide patients and healthcare providers with timely access to transformative medical devices by speeding up their development, assessment and review, while preserving the statutory standards for premarket approval. Eligibility is restricted to innovative medical devices that provide more effective treatment or diagnosis of life-threatening conditions, where there are no approved or cleared alternatives, and where early device availability is in the best interests of patients.

To achieve Breakthrough Device Status a panel of experts at the FDA extensively reviewed both RESPMETER and its prospective users. Following the confirmation of this designation, the company will now receive additional support from the FDA, and any submission for US approval of RESPMETER will be reviewed as a priority.