6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC)
FDA 510(k)
FDA Class 2
·General Hospital
DUAL LUMEN CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Arrow Epidural Catheter Kit
FDA 510(k)
FDA Class 2
·Anesthesiology
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·November 11, 2014
VIRTUOSO VR
FDA Adverse Event
Malfunction
·MEDTRONIC S.A.·Product code LWS·September 12, 2011
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 23, 2013