27 results
·
33ms
·
Sources: EU EUDAMED, US FDA
LIFEPAK 600 AUTOMATED EXTERNAL DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040014158·Zirlux 16+ A1 98.5X22
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00031568573316·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00031568573323·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00070135573328·
CORINNE MCCORMACK INC.
FDA UDI
FGX INTERNATIONAL INC.·00193033265598·
CORINNE MCCORMACK INC.
FDA UDI
FGX INTERNATIONAL INC.·00193033265628·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00070135573267·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00070135573311·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00031568573262·
CORINNE MCCORMACK INC.
FDA UDI
FGX INTERNATIONAL INC.·00193033265611·
TEXTURED POWDER-FREE LATEX EXAMINATION GLOVES WITH CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER
FDA 510(k)
FDA Class 1
·General Hospital
ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS
FDA 510(k)
FDA Class 1
·Ophthalmic
16CM MIN. INVASIVE ATTACHMENT
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code HBC·March 29, 2013
BONE SCREW 76353200 REPOSE SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code LRK·December 12, 2012
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·March 15, 2013
UNICEL® DXC 800 SYNCHRON® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JGS·March 8, 2011
VICTORY XL SR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2008
EMAX 2 MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 6, 2015
8CM ANGLE ATTACHMENT, BLACK, MAX
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 9, 2014