10,000 results
·
130ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TRILOGY O2
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·December 22, 2016
VELA VENTILATOR
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code CBK·December 27, 2016
980 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·October 24, 2016
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·October 26, 2016
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·October 27, 2016
980 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·November 2, 2016
VELA VENTILATOR
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code CBK·November 3, 2016
V200 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·October 25, 2016
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·November 30, 2016
980 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·November 30, 2016
EVITA 4
FDA Adverse Event
Malfunction
·DRÄGERWERK AG & CO. KGAA·Product code CBK·December 7, 2016
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 16, 2016
840 VENTILTOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·December 16, 2016
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code CBK·December 2, 2016
UNI-VENT MODEL 731
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code CBK·December 13, 2016
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·December 13, 2016
TRILOGY 202
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·December 13, 2016
UNI-VENT MODEL 731
FDA Adverse Event
Malfunction
·IMPACT PRODUCTS·Product code CBK·December 13, 2016
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·December 5, 2016
HT70
FDA Adverse Event
Malfunction
·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·December 19, 2016