8 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
NUCLEUS 22
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·May 18, 2025
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD .·Product code MCM·February 24, 2015
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD .·Product code MCM·February 20, 2015
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD .·Product code MCM·March 27, 2015
OLYMPUS HF-RESECTION ELECTRODE
FDA Adverse Event
OLYMPUS WINTER & IBE GMBH·Product code FJL·April 21, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code LZG·November 1, 2010