45 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BACK-UP MEIER GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810119061·Schein Alginate 20# drum
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810119069·Schein Alginate 20# drum
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00193033440254·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0112060·Tap, 6.50mm
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112060·Tap, 8.5 mm
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00193033440261·
InSePtion MIS Fixation System
FDA UDI
Kalitec Direct LLC·B07314K0112060·Punch, 6 and 8 mm
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00193033440247·
MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254
FDA 510(k)
FDA Class 2
·Cardiovascular
ELECSYS INSULIN CALSET
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·March 27, 2007
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code DQY·December 28, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·March 5, 2007
PYRAMESH C TITANIUM MESH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code EZX·August 12, 2011
PYRAMESH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code EZX·September 29, 2015
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 28, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code DQY·April 12, 2007
ASTERX EXPANDABLE CORPECTOMY SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019