7 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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VARIPULSE¿ BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code QZI·May 21, 2026
IAB: 7.5 FR - 40 CC
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·November 3, 2014
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 8, 2011
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·July 11, 2013
TRUPULSE¿ GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code QZI·December 1, 2025
GIA
FDA Adverse Event
Injury
·US SURGICAL PUERTO RICO·Product code GDW·June 15, 2023
TRUPULSE¿ GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code QZI·April 21, 2026