6 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
*
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS DIV. OF STRYKER CORPORATION·Product code HBE·February 24, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 31, 2014
XIA TITANIUM 4.5 TA6V LONG ROD DIAM 4.5 X 200
FDA Adverse Event
Injury
·STRYKER SPINE BORDEAUX·Product code KWP·November 14, 2012
RESTORE ULTRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 21, 2010
TECNIS
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code MFK·March 11, 2016
CEEON
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·March 14, 2016