37 results · 23ms · Sources: EU EUDAMED, US FDA

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APEEL CS PLUS CATHETER DELIVERY SYSTEM, MODELS 407579, 407580, 407581, 407582

FDA 510(k)
FDA Class 2 ·Cardiovascular

ABBOTT ACCLAIM ENCORE, MODEL 12237

FDA 510(k)
FDA Class 2 ·General Hospital

BURR HOLE COVER, MODEL XX

FDA 510(k)
FDA Class 2 ·Neurology

COBALT HV BN CMT 40G-JAPAN

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code LOD·July 29, 2016

REFOBACIN PLUS BONE CEMENT 40

FDA Adverse Event
Death ·BIOMET FRANCE S.A.R.L·Product code LOD·December 3, 2015

REFOBACIN BONE CEMENT R 40X2 GERMAN

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L·Product code LOD·November 23, 2015

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 22, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 23, 2016

OPTIPAC SOFTPAC HIPSET

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 25, 2016

OPTIPAC-S 60 REFOB BN CMT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 25, 2016

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 23, 2016

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

OPTIPAC-S 80 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 6, 2016

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 7, 2016

OPTIPAC-S 80 REFOBACIN PLUS BONE CEMENT

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 5, 2016

VIRTUOSO DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·April 10, 2013

VERSYS HIP SYSTEM FEMORAL STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LPH·April 5, 2011

DEEP BRAIN STIMULATION LEAD

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·May 22, 2008