7 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MULTI-LUMEN INTRAVENOUS INFUSION CATH
FDA 510(k)
FDA Class 2
·Cardiovascular
ORTHOPACS
FDA 510(k)
FDA Class 2
·Radiology
Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
M2A-MAGNUM PF CUP 50ODX44ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 27, 2014
INTERSTIM II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code EZW·November 15, 2012
EVOLIS MICROPLATE SYSTEM
FDA Adverse Event
Other
·BIO-RAD LABORATORIES, INC·Product code JTC·September 3, 2010
Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018