3 results
·
19ms
·
Sources: EU EUDAMED, US FDA
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FDA Adverse Event
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FDA Adverse Event
Malfunction
·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·April 18, 2014
ASR 300 SPIKED CUP SIZE 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·September 26, 2012
PRECISION XTRA
FDA Adverse Event
Injury
·Product code NBW·July 16, 2010