11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SP-LINK System
FDA 510(k)
FDA Class 2
·Orthopedic
ZenFlex
FDA UDI
Kerr Corporation·00195062029905·Rotary Files
SERIM DISINTEK OPA TEST STRIP
FDA 510(k)
FDA Class 2
·General Hospital
EVOLVE EPS ORTHOLOC
FDA 510(k)
FDA Class 2
·Orthopedic
COOK CVC TRIPLE LUMEN POWER-INJECTABLE CENTRAL VENOUS CATHETER TRAY
FDA Adverse Event
Malfunction
·COOK INC·Product code FOZ·October 21, 2024
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 10, 2013
FREESTYLE 100 TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC.·Product code NBW·July 25, 2011
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 8, 2014
COOK CVC TRIPLE LUMEN POWER-INJECTABLE CENTRAL VENOUS CATHETER TRAY
FDA Adverse Event
Malfunction
·COOK INC·Product code FOZ·March 29, 2024
COOK CVC TRIPLE LUMEN POWER-INJECTABLE CENTRAL VENOUS CATHETER TRAY
FDA Adverse Event
Malfunction
·COOK INC·Product code FOZ·March 28, 2024
COOK CVC SINGLE LUMEN CENTRAL VENOUS CATHETER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FOZ·December 28, 2023