8 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PENUMA IMPLANT
FDA Adverse Event
Injury
·NATIONAL MEDICAL DEVICES INC.·Product code MIB·March 1, 2018
ASSURANT COBALT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIO·April 9, 2013
EON MINI IPG, 16-CHANNEL RECHARGEABLE
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 31, 2011
CONTAK RENEWAL 3 RF
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008
INTERSTIM
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code EZW·February 21, 2020
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·January 6, 2022
HAHN TAPERED IMPLANT Ø3.5 X 8 MM
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·November 1, 2021
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·January 6, 2022