6 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DRIVE SHAFT-MINIMUM 360MM LENGTH-FOR USE WITH RIA
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTO·January 23, 2023
MONO BENDABLE ONE PIECE IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 27, 2024
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 16, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 27, 2013
COBAS® TAQMAN® 48 ANALYZER
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS, LTD.·Product code JJF·February 24, 2011
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 19, 2008