20 results · 42ms · Sources: EU EUDAMED, US FDA

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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