3 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
U1105 S1000 TINA HD WITH NIBP
FDA Adverse Event
Death
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·December 2, 2008
S8 AUTOSET SPIRIT
FDA Adverse Event
Malfunction
·RESMED LTD.·Product code BZD·August 31, 2011
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 29, 2013