10 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Z - SERIES MODULAR TOTAL HIP SYSTEM PLASMA COATED
FDA 510(k)
FDA Class 2
·Orthopedic
CHARTER MEDICAL NEONATAL SYRINGE SET
FDA 510(k)
FDA Class 2
·General Hospital
MODIFICATION TO MILLER/GALANTE PRECOAT UNICOMPARTMENTAL KNEE SYSTEM (8 MM ARTICULAR SURFACE)
FDA 510(k)
FDA Class 2
·Orthopedic
SUNDT INTERNAL CAROTID SHUNT
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES, INC.·Product code DWF·October 29, 2004
FINELINE II
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVN·April 8, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 22, 2011
CONTOUR TS TEST STRIPS (50)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·May 8, 2008
BD LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·June 15, 2023
BD LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·June 15, 2023
The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018