7 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ROTACLONE ROTAVIRUS DIAGNOSTIC KIT
FDA 510(k)
FDA Class 1
·Microbiology
SLENDERTONE GYMBODY, MODEL 512-01
FDA 510(k)
FDA Class 2
·Physical Medicine
ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY
FDA 510(k)
FDA Class 2
·General Hospital
MIS PEDICLE SCREW PERCUTANOUS TOWER ENH. JPN
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·March 8, 2019
FREESTYLE NAVIGATOR
FDA Adverse Event
Malfunction
·Product code LFR·October 5, 2010
TALENT THORACIC STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·November 30, 2012
UNKNOWN_CORK_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWA·June 6, 2014