6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DUOTIP-TEST
FDA 510(k)
FDA Class 2
·General Hospital
SOLO-CARE AQUA ANTIMICROBIAL LENS CASE
FDA 510(k)
FDA Class 2
·Ophthalmic
JAGWIRE HIGH PERFORMANCE GUIDWIRE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ULTRAFLEX ESOPHAGEAL STENT SYSTEM, ULTRAFLEX DIAMONDBILIARY STENT SYSTEM, ULTRAF
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code JCT·December 30, 2010
BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code MBI·July 17, 2014
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 21, 2012