4 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SWINFORD·Product code KDI·June 16, 2014
KAPPA 600 DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·October 19, 2010
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code MMI·December 15, 2012
OSTYCUT BONE BIOPSY NEEDLE
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015