7 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CEEON
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, GRONINGEN·Product code HQL·December 23, 2002
CEEON
FDA Adverse Event
Injury
·PHARMACIA & UPJOHN, GRONINGEN·Product code HQL·December 23, 2002
DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SWINFORD·Product code KDI·March 27, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·March 18, 2011
MTOME ST HOLSTER/CABLES
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code KNW·March 27, 2008
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·December 23, 2025
PANEL PHOENIX NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 22, 2023