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Anesthesia & Respiratory Devices

Sunovion gets FDA approval for Lonhala Magnair inhalation solution to treat COPD Sunovion Pharmaceuticals announced that the US Food and Drug Administration (FDA) has approved the new drug application (NDA) for Lonhala Magnair (glycopyrrolate) inhalation solution (25 mcg twice daily), also known as SUN-101/eFlow, for the long-term, maintenance treatment of airflow obstruction in people with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or emphysema.
Specialty Devices > Anesthesia & Respiratory Devices > News
FDA approves first electronic device for opioid withdrawal therapy The US Food and Drug Administration (FDA) has granted permission to Innovative Health Solutions to market bridge neurostimulation system NSS-2 Bridge, the first device for use in helping to reduce the symptoms of opioid withdrawal.
Specialty Devices > Anesthesia & Respiratory Devices > News Hollister begins construction on new manufacturing plant in Lithuania Hollister Incorporated, a global medical device manufacturer, held a groundbreaking ceremony signifying the start of construction on a manufacturing plant in the Kaunas FEZ (Free Economic Zone) region of Lithuania.
Specialty Devices > Anesthesia & Respiratory Devices > News
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