337 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARPX
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARP(X)TM NEEDLE DESTRUCTION UNIT
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARPX NEEDLE DESTRUCTION UNIT
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARP NEEDLE DESTRUCTION UNIT
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARP NEEDLE DESTRUCTION UNIT
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARPX NEEDLE DESTRUCTION UNIT
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980015·DeltaForm HighDefinition posterior; shade A2; s...
THE HEART LASER CO2 TMR SYSTEM (P950015)
FDA Adverse Event
Injury
·NOVADAQ TECHNOLOGIES,=INC.·Product code MNO·September 8, 2013
FRESENIUS 2008K
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 22, 2013
LIVIAN
FDA Adverse Event
Death
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·February 7, 2011
VIRTUOSO VR
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA·Product code LWS·April 10, 2018
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 9, 2016
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
ADAPTA D
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, PLC·Product code DXY·March 27, 2015
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·June 9, 2015
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·March 27, 2015
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·May 1, 2018
MEDTRONIC LEAD
FDA Adverse Event
Injury
·MEDTRONIC, PLC·Product code DXY·March 27, 2015