7 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNI-POLAR HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
Precept
FDA UDI
Nuvasive, Inc.·00887517387592·PRECEPT Screw Shank, 6.5x80mm Modular
LIPID STOPCOCK
FDA 510(k)
FDA Class 2
·Cardiovascular
INTRAVASCULAR CATHETER WITH HYDROPHILIC COATING
FDA 510(k)
FDA Class 2
·Cardiovascular
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 16, 2014
PASSIVE PLUS DX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010
PARIETEX UGYTEX PP POSTERIOR KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code FTL·December 13, 2012