8 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BriefCase-Quantification
FDA 510(k)
FDA Class 2
·Radiology
BD SYRINGE LUER-LOK TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 18, 2020
STEREOTACTIC BODY FRAME, MODEL COD. 70-1A
FDA 510(k)
FDA Class 2
·Radiology
VersaWrap Nerve Protector
FDA 510(k)
FDA Class 2
·Neurology
GATEWAY PTA DILATION CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code GBA·November 14, 2008
CLARION
FDA Adverse Event
Malfunction
·ADVANCED BIONICS, LLC·Product code MCM·August 22, 2011
PELVICOL 2CM X 7CM 1.0MM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TISSUE·Product code FTL·July 12, 2013
Revogene, Catalog no. 610210. IVD test instrument
FDA Enforcement
Class II
·Ongoing·Meridian Bioscience Inc·August 3, 2022