6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VIBRACARE
FDA 510(k)
FDA Class 1
·Physical Medicine
SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Supplemental Instrument Trays
FDA 510(k)
FDA Class 2
·General Hospital
UNKNOWN DEPUY ASR ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·June 12, 2014
ANEURX AAADVANTAGE STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·October 8, 2010
PROMUS ELEMENT ¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 12, 2012