7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CADD SOLIS HPCA AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code MEA·December 23, 2024
CONSTRAINED TIBIAL ARTICULAR SURFACE PROVISIONAL RIGHT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code MBH·August 15, 2018
PS TIBIAL ARTICULAR SURFACE PROVISIONAL LEFT SIZE 6-9 GH TOP
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·August 15, 2018
PUMP MMT-515NAS PRDGM INS V2.1 SK EN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MEDL-REL·Product code OYC·November 12, 2007
PUMP,COLLEAGUE SINGLE CHANNELCOLOUR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·April 5, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·May 7, 2008
BD INSYTE¿ IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·March 3, 2020