20 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011
MARY HITCHCOCK HANOVER NH 1
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·November 7, 2012
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS INC·Product code LNM·November 4, 2011
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC (FORMALLY BIOFORM MEDICAL, INC)·Product code LNM·October 29, 2010
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC. (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS INC·Product code LNM·November 4, 2011
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 10, 2013
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 31, 2011
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·May 8, 2008
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
PRECISE PRO RX OUS CAROTID SYSTEM, 5F, 8MM X 30MM, 135 CM
FDA Adverse Event
Malfunction
·CORDIS CORPORATION·Product code NIM·February 2, 2018