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Anesthesia & Respiratory Devices News

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121-135 of 668 results
CardiacAssist’s PROTEK Duo veno-venous cannula receives Health Canada approval
By MDBR Staff Writer
Health Canada has granted Class 2 medical device license for CardiacAssist’s new PROTEK Duo veno-venous cannula.
Specialty Devices > Anesthesia & Respiratory Devices > News
Westmed’s Vibralung Acoustical Percussor receives FDA approval
By MDBR Staff Writer
Medical device company Westmed has received 510(k) approval from the US Food and Drug Administration (FDA) for its Vibralung Acoustical Percussor.
Specialty Devices > Anesthesia & Respiratory Devices > News
Liberia hospitals deploy TRU-D SmartUVC to fight against Ebola virus
By MDBR Staff Writer
The JFK Hospital and ELWA Hospital in Monrovia, Republic of Liberia, have deployed two 5ft superbug-slaying machines from the US to aid in the fight against the Ebola virus outbreak.
Specialty Devices > Anesthesia & Respiratory Devices > News
PDI subsidiary Interpace Diagnostics enters molecular diagnostics market with thyroid and pancreatic cancer test portfolio acquisition
PDI, a leading healthcare commercialization company, announced that its Interpace Diagnostics subsidiary has entered the expanding cancer molecular diagnostics market with the acquisition of the miRInform Thyroid and Pancreas cancer test assets from privately held Asuragen.
Specialty Devices > Anesthesia & Respiratory Devices > News
ITC rules redesigned APEX humidifier still infringes ResMed patents
An International Trade Commission (ITC) ruling issued Friday held that, despite a redesign of its iCH CPAP device, Taiwanese device manufacturer APEX continues to infringe ResMed patents in its humidification.
Specialty Devices > Anesthesia & Respiratory Devices > News
Merit Medical Systems gains Chinese approval for Aero tracheobronchial stent system
By MDBR Staff Writer
Merit Medical Systems, a US-based medical device company, has obtained approval from the Chinese Food and Drug Administration (CFDA) for its Aero tracheobronchial stent system.
Specialty Devices > Anesthesia & Respiratory Devices > News
Inova Labs obtains FDA approval for Activox DUO2 oxygen concentrator system
By MDBR Staff Writer
Inova Labs, a manufacturer of oxygen therapy solutions, has obtained approval from the US Food and Drug Administration (FDA) for its Activox DUO2 oxygen concentrator system.
Specialty Devices > Anesthesia & Respiratory Devices > News
Inogen announces FDA clearance of home oxygen concentrator
Inogen has received the US Food and Drug Administration (FDA) clearance for an home oxygen concentrator called the Inogen At Home.
Specialty Devices > Anesthesia & Respiratory Devices > News
Smiths Medical launches tracheostomy tubes for neonates and pediatric patients in Europe
Smiths Medical, a medical device manufacturer, has announced that its Portex Bivona FlexTend TTS tracheostomy tubes will now be included in the company’s standard product offering for European countries.
Specialty Devices > Anesthesia & Respiratory Devices > News
FDA approves Itamar Medical’s WatchPAT Unified sleep apnea diagnostic device
By MDBR Staff Writer
Itamar Medical has received approval from the US Food and Drug Administration (FDA) for its new and upgraded model of the WatchPAT sleep apnea diagnostic device, WatchPAT Unified.
Specialty Devices > Anesthesia & Respiratory Devices > News
CFDA approves Dehaier Medical’s Morpheus Ox sleep diagnostic software
By MDBR Staff Writer
Dehaier Medical Systems has obtained the China Food and Drug Administration’s (CFDA) approval for its Morpheus Ox sleep diagnostic software.
Specialty Devices > Anesthesia & Respiratory Devices > News
Covidien announces European launch of Nellcor respiration rate system
By MDBR Staff Writer
Covidien, a global healthcare products company, has announced CE Mark approval and the commercial launch of its Nellcor respiration rate system in Europe.
Specialty Devices > Anesthesia & Respiratory Devices > News
FDA approves Advanced Brain Monitoring’s positional obstructive sleep apnea device
By MDBR Staff Writer
US-based medical device company Advanced Brain Monitoring has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Night Shift, a therapy for positional obstructive sleep apnea.
Specialty Devices > Anesthesia & Respiratory Devices > News
Masimo announces CE Mark of iSpO2 Rx pulse oximeter for mobile devices
Masimo has announced that the iSpO2 Rx pulse oximeter for Android and iOS devices has received CE Mark clearance for medical use in select countries, offering clinicians the power of Masimo SET Measure-through Motion and Low Perfusion pulse oximetry on their smart phones and tablets.
Specialty Devices > Anesthesia & Respiratory Devices > News
CAS Medical Systems and Century Medical execute distribution agreement for Fore-Sight oximeters in Japan
CAS Medical Systems has signed an agreement with Century Medical to serve as the exclusive distributor of the company's Fore-Sight Elite cerebral oximeters in Japan.
Specialty Devices > Anesthesia & Respiratory Devices > News
121-135 of 668 results