37 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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