Log in or Register for enhanced features | Forgotten Password?
White Papers | Suppliers | Events | Report Store | Companies | Dining Club | Videos
Specialty Devices
Anesthesia & Respiratory Devices
Return to: MDBR Home | Specialty Devices | Anesthesia & Respiratory Devices | News
Search Refinements

Anesthesia & Respiratory Devices News

View news from other Medical Devices sectors:
136-150 of 667 results
MGC Diagnostics, Neurovirtual sign distribution deal for sleep apnea diagnostic products
By MDBR Staff Writer
Global medical technology company MGC Diagnostics and Neurovirtual USA have entered into an agreement under which MGC Diagnostics will market and distribute the SleepVirtual BWII PSG and BWIII PSG diagnostic polysomnography systems in the US and Canada.
Specialty Devices > Anesthesia & Respiratory Devices > News
ResMed launches new life support ventilators
By MDBR Staff Writer
ResMed, a medical device company, has announced the launch of its Astral 100 and Astral 150 life support ventilators in select European and Asia-Pacific markets.
Specialty Devices > Anesthesia & Respiratory Devices > News
Propeller Health obtains FDA 510(k) clearance for next generation Propeller platform
By MDBR Staff Writer
Propeller Health has obtained 510(k) clearance from the US Food and Drug Administration (FDA) for its next generation Propeller platform, which includes a new low-energy sensor that eliminates charging.
Specialty Devices > Anesthesia & Respiratory Devices > News
FDA approves Inspire upper airway stimulation therapy for obstructive sleep apnea
Inspire Medical Systems has announced that the US Food and Drug Administration (FDA) has approved Inspire upper airway stimulation (UAS) therapy for use in a subset of patients with moderate to severe obstructive sleep apnea (OSA) who are unable to use continuous positive airway pressure (CPAP).
Specialty Devices > Anesthesia & Respiratory Devices > News
Smiths Medical introduces Pneupac paraPAC plus in US, Canada
By MDBR Staff Writer
Smiths Medical, a US-based global medical device manufacturer, has launched its Pneupac paraPAC plus ventilator in the US and Canada.
Specialty Devices > Anesthesia & Respiratory Devices > News
Breathe Technologies obtains fifth FDA approval for NIOV system
By MDBR Staff Writer
Breathe Technologies has obtained the fifth 510(k) clearance from the US Food and Drug Administration (FDA) for its non-invasive open ventilation (NIOV) system, allowing its use with compressed air supply for non-oxygen dependent patients.
Specialty Devices > Anesthesia & Respiratory Devices > News
OxySure’s model 615 portable emergency oxygen device gets CE Mark approval
By MDBR Staff Writer
OxySure Systems has obtained CE mark approval for its OxySure Model 615 portable emergency oxygen device, designed to administer medical oxygen easily and quickly in any medical emergency, while waiting for paramedics or first responders to arrive on the scene.
Specialty Devices > Anesthesia & Respiratory Devices > News
AirWare Labs announces manufacturing and sales expansion into China
AirWare Labs has announced plans to expand manufacturing, distribution and sales of its AIR filtered nasal products in China.
Specialty Devices > Anesthesia & Respiratory Devices > News
MGC Diagnostics signs letter of intent to acquire Medisoft
By MDBR Staff Writer
Global medical technology company MGC Diagnostics has signed a letter of intent to acquire Medisoft, a Belgium-based cardio-respiratory diagnostics products manufacturer.
Specialty Devices > Anesthesia & Respiratory Devices > News
Nonin Medical adds new programming features to wrist-worn pulse oximeter
By MDBR Staff Writer
US-based Nonin Medical has announced the addition of a memory volume indicator (MVI) mode to its WristOx2 Model 3150 wrist-worn pulse oximeter.
Specialty Devices > Anesthesia & Respiratory Devices > News
Flagler Hospital upgrades to Masimo SET pulse oximetry for improved patient outcomes
Masimo has announced that Flagler Hospital has upgraded system-wide to Masimo SET pulse oximetry, the standard-of-care at leading hospitals around the world.
Specialty Devices > Anesthesia & Respiratory Devices > News
Covidien obtains CE Mark approval for Puritan Bennett 980 ventilator
By MDBR Staff Writer
Covidien has obtained European Economic Area (EEA) CE Mark approval approval for its Puritan Bennett 980 ventilator, which helps patients to breathe more naturally through some of the most innovative breath technology available.
Specialty Devices > Anesthesia & Respiratory Devices > News
Boehringer Ingelheim says new Phase III data show tiotropium Respimat effective across asthma severities
Boehringer Ingelheim has announced new data from large scale, Phase III studies showing that once-daily tiotropium delivered via the Respimat inhaler was effective and well tolerated in patients across asthma severities.
Specialty Devices > Anesthesia & Respiratory Devices > News
FDA issues class I recall for GE Healthcare’s resuscitation systems
By MDBR Staff Writer
GE Healthcare has recalled its Giraffe and Panda Warmer Infant Resuscitation systems as the oxygen and air wall inlet fittings on the back panel of the resuscitation systems were reversed during assembly.
Specialty Devices > Anesthesia & Respiratory Devices > News
Covidien obtains FDA 510(k) approval for Puritan Bennett 980 ventilator
By MDBR Staff Writer
Ireland-based Covidien has obtained 510(k) approval from the US Food and Drug Administration (FDA) for its Puritan Bennett 980 ventilator, which helps patients to breathe more naturally through some of the most innovative breath technology available.
Specialty Devices > Anesthesia & Respiratory Devices > News
136-150 of 667 results