41 results
·
30ms
·
Sources: EU EUDAMED, US FDA
NORWOOD ABBEY CENTURION SES EPIKERATOME
FDA 510(k)
FDA Class 1
·Ophthalmic
Q-RAD RADIOGRAPHIC SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
GENX CODA AIR PURIFICATION SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
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
PENUMBRA SYSTEM 5MAX SEPARATOR
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·April 10, 2013
SHUNT SENSOR SYS500
FDA Adverse Event
TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DRY·March 31, 2011
CELL-DYN SAPPHIRE ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 21, 2008