4 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ZILVER PTX 35 DRUG-ELUTING STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIU·May 20, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 27, 2012
PORTEX 8.0 CUFFED TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL LTD.·Product code BTO·September 21, 2010
5.5 HEALIX3 PEEK ANC.W/OCORD
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·January 17, 2019