7 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
IOLMASTER 500
FDA Adverse Event
Malfunction
·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·October 14, 2015
OSSTELL SMARTPEG TYPE 101, 102, 103, 104
FDA Adverse Event
Malfunction
·OSSTELL AB·Product code EKX·May 15, 2025
ENROUTE TRANSCAROTID NEUROPROTECTION SYSTEM
FDA Adverse Event
Injury
·SILK ROAD MEDICAL·Product code NTE·August 11, 2025
DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 9, 2013
GRANUFLEX/DUOACTIVE MOISTURE RETENTIVE DRSG
FDA Adverse Event
Injury
·CONVATEC, INC.·Product code NAD·September 17, 2014
OT ULTRALINK METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 24, 2011
OCTOPUS 3 TISSUE STABILIZER
FDA Adverse Event
Death
·PERFUSION SYSTEMS·Product code MWS·February 4, 2021