3 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PFC*SIGMA/RD/DOME PAT 3PEG,35
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012
EON IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·August 6, 2010