6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRIMALOC CEMENTLESS HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BETA-TSH-IRMA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
AKROTECH 4000
FDA 510(k)
FDA Class 2
·Physical Medicine
LIFEVEST WCD 3100 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·January 15, 2013
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM.
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·July 23, 2014