6 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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E-Z FIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CARDIOSLEEVE
FDA 510(k)
FDA Class 2
·Cardiovascular
STERI-DRAPE SURGICAL DRAPES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AUTOPULSE® LI-ION BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC·Product code DRM·May 23, 2014
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 6, 2012
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code MDS·September 10, 2010