10,000 results
·
22ms
·
Sources: EU EUDAMED, US FDA
SGW Technik GmbH
Manufacturer
🇩🇪 Germany
CINCH QR SGW EXTENSION
FDA 510(k)
FDA Class 2
·Cardiovascular
PKIT, AXIS, LPV, SG, W/TUBING
FDA UDI
MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430114960·
PKIT, AXIS, LPV, SG, W/TUBING
Device
EU MDR
·
Eu Md Class 1
·Mizuho Orthopedic Systems, Inc.·On the market
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Malfunction
·CORDIS LLC (PR)·Product code NIQ·April 27, 2005
EXTRA BACK-UP 3.5
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code DYB·April 27, 2005
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Malfunction
·CORDIS LLC (PR)·Product code NIQ·April 27, 2005
PKIT, AXIS, 5 IN. GT, SG, W/TUBING
FDA UDI
MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430114243·
PKIT, AXIS, LPV, SG, W/TUBING, 6/CS
Device
EU MDR
·
Eu Md Class 1
·Mizuho Orthopedic Systems, Inc.·On the market
PKIT, AXIS, 5 IN. GT, SG, W/TUBING
Device
EU MDR
·
Eu Md Class 1
·Mizuho Orthopedic Systems, Inc.·On the market
PKIT, AXIS, LPV, SG, W/TUBING (3/CS)
Device
EU MDR
·
Eu Md Class 1
·Mizuho Orthopedic Systems, Inc.·On the market
SHINOBI SGW
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code DQX·March 22, 2010
ATW GUIDEWIRE
FDA Adverse Event
Malfunction
·CORDIS CORPORATION·Product code DQX·September 26, 2012
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268108424·Guidewire
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268100541·Guidewire
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268110083·Guidewire
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268109698·Guidewire
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268109667·Guidewire
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268101173·Guidewire
Guidewire
FDA UDI
GALT MEDICAL CORP.·00841268109650·Guidewire