47 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REM440
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
CEDIA DAU AMPHETAMINES/ECSTASY ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
EVERSHEARS BIPOLAR SCISSORS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COBALT HV BN CMT 40G-JAPAN
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code LOD·July 29, 2016
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
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
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 8, 2013
TENDRIL DX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008