39 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAREVENT ATV+ AND CAREVENT MRI
FDA 510(k)
FDA Class 2
·Anesthesiology
N/A
FDA UDI
GEORGE TIEMANN & CO.·B58210514690·
MINOLTA PULSOX-2
FDA 510(k)
FDA Class 2
·Cardiovascular
R&D PROJECT DW269#25
FDA 510(k)
FDA Class 2
·Dental
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
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 10, 2013
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·May 21, 2008