876 results
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76ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FACEFIT AND FACEFIT PORTED NON-INVASIVE VENTILATION MASKS
FDA 510(k)
FDA Class 2
·Anesthesiology
PNEUTON MINI VENTILATOR PNEUTON MINI NON-INVASIVE VENTILATION (NIV) KIT ACCESSORY
FDA 510(k)
FDA Class 2
·Anesthesiology
NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474
FDA 510(k)
FDA Class 2
·Anesthesiology
NON-INVASIVE VENTILATOR
FDA Adverse Event
Injury
·UNK·Product code CBK·August 23, 2023
NON - INVASIVE VENTILATOR
FDA Adverse Event
Malfunction
·PHILLIPS RESPIRONICS·Product code MNT·November 23, 2016
NON - INVASIVE VENTILATOR
FDA Adverse Event
Malfunction
·PHILLIPS RESPIRONICS·Product code MNT·November 23, 2016
*
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·June 18, 2013
REVEL
FDA Adverse Event
Death
·CAREFUSION 203, INC·Product code CBK·October 25, 2012
BELLAVISTA
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·September 22, 2025
BIPAP A30
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·May 8, 2025
BIPAP S/T CSERRIES
FDA Adverse Event
Injury
·PHILIPS RESPIRONICS, INC.·Product code MNS·November 17, 2021
V60 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 23, 2017
PREFILLED HUMIDIFIER
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code BTT·January 30, 2003
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·May 19, 2026
BIPAP A30, CHINA
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·June 4, 2025
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·March 9, 2023
980 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·May 29, 2015
MICROVENT
FDA Adverse Event
Death
·DRAGER MEDIZINTECHNIK GMBH·Product code CBK·November 17, 2000
BASE UNIT SERVO-U
FDA Adverse Event
Injury
·MAQUET CRITICAL CARE AB·Product code CBK·May 11, 2026
BASE UNIT SERVO-U
FDA Adverse Event
Injury
·MAQUET CRITICAL CARE AB·Product code CBK·May 11, 2026