8 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
NUCLEUS 22
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·May 18, 2025
PENUMBRA COIL 400
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·April 24, 2017
PX SLIM DELIVERY MICROCATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·April 24, 2017
DLT TS CER HD 12/14 36MM +8.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LZO·April 25, 2019
UNICEL DXC 800 PRO SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JJE·May 30, 2014
MEDTRONIC INFUSE BONE GRAFT OR RHBMP2
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NEK·November 15, 2012
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 12, 2015