10 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH SLIM MODIOLAR ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·February 13, 2026
COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH CONTOUR ADVANCE® ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·February 13, 2026
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·May 24, 2013
COCHLEAR OSIA OSI300 IMPLANT
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code PFO·January 15, 2024
NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code PGQ·July 4, 2016
NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code PGQ·August 1, 2016
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
MEDEL S.P.A.·Product code BTI·February 20, 2013
TERUMO SOFT FLOW CANNULAE
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWF·January 14, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 31, 2014
PULSE GEN MODEL 1000
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code LYJ·September 7, 2022