3 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
12/14 ARTICUL 40MM M SPEC+1.5
FDA Adverse Event
Injury
·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code LPH·June 10, 2014
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 11, 2010
2.4/2.7MM VA-LCP FIRST TMT FUSION PLATE/STANDARD
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HRS·December 10, 2012