4 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
TRILOGY 200
FDA Adverse Event
Malfunction
·RESPIRONICS INC·Product code CBK·August 19, 2020
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 3, 2013
ADULT OPEN HEART PACK W/HMO 71000
FDA Adverse Event
Malfunction
·DATASCOPE CORP·Product code DTZ·August 21, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·PURITAN BENNETT CORP.·Product code CBK·April 15, 2011