10,000 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CENTRAL BODY F/MEF MAX-L 437 MIN-L 287
FDA Adverse Event
Injury
·SYNTHES HAGENDORF·Product code HST·March 8, 2016
O-RING F/392.901
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HST·March 8, 2016
O-RING F/392.901
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HST·March 8, 2016
RADIESSE DERMAL FILLER
FDA Adverse Event
Injury
·BIOFORM MEDICAL·Product code LMH·January 23, 2008
STD-CLAMP F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 12, 2018
STD-CLAMP F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·November 26, 2018
STD-CLAMP F/MEF
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·June 24, 2013
STD-CLAMP F/MEF
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·June 25, 2013
STD-CLAMP F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 12, 2018
SLEEV 2PART L50 F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018
SLEEV 2PART L50 F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018
SLEEV 2PART L50 F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·October 12, 2018
SLEEV 2PART L50 F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·October 12, 2018
SLEEVE F/SEGM-TRANSP F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018
SLEEVE F/SEGM-TRANSP F/MEF
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·October 12, 2018
SLEEVE F/SEGM-TRANSP F/MEF
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·February 28, 2019
DRILLSL 7/6 LONG F/MEF
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZX·June 23, 2025
DRILLSL 7/6 LONG F/MEF
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZX·June 23, 2025
DRILLSL 7/6 LONG F/MEF
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZX·June 23, 2025
CARDIAC CATHETER
FDA Adverse Event
Injury
·Product code DRF·February 11, 2016