39 results · 24ms · Sources: EU EUDAMED, 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