5 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LUMA ARCH
FDA Adverse Event
Injury
·LUMALITE, INC.·Product code EEG·July 6, 2004
VERSAFITCUP DM DOUBLE MOBILITY HC LINER 50/28
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MEH·May 17, 2021
ATLAS MONITOR
FDA Adverse Event
Malfunction
·WELCH ALLYN PROTOCOL, INC.·Product code DQA·February 13, 2013
LIFEVEST WCD 3100 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·February 9, 2011
ACCU-CHEK AVIVA
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·February 8, 2008