459 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
1920664-1997-00200
FDA Adverse Event
Malfunction
·Product code HQE·April 14, 1997
1920664-2003-00239
FDA Adverse Event
Malfunction
·Product code ---·May 2, 2003
1920664-1997-00052
FDA Adverse Event
Malfunction
·Product code HQE·January 17, 1997
1920664-1997-00459
FDA Adverse Event
Malfunction
·Product code HQE·October 8, 1997
1920664-1997-00461
FDA Adverse Event
Malfunction
·Product code HQE·October 8, 1997
1920664-1997-00460
FDA Adverse Event
Malfunction
·Product code HQE·October 8, 1997
1920664-1997-00458
FDA Adverse Event
Malfunction
·Product code HQE·October 8, 1997
*
FDA Adverse Event
Malfunction
·Product code HQC·October 3, 1996
STELLARIS 25GA POSTERIOR PACK W WF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·May 14, 2013
STELLARIS 25GA POSTERIOR PACK W WF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·May 14, 2013
STELLARIS 25GA POSTERIOR PACK W WF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·May 14, 2013
STELLARIS 25GA POSTERIOR PACK W WF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·May 14, 2013
STELLARIS 25G VITRECTOMY CUTTER
FDA Adverse Event
Malfunction
·BAUSCH + LOMB, INC.·Product code HQC·October 3, 2013
STELLARIS 25G VITRECTOMY CUTTER
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·October 3, 2013
STELLARIS MICRO INCISION VACUUM PK 6/BX
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·July 17, 2014
STELLARIS MICRO INCISION VACUUM PK 6/BX
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·July 17, 2014
STELLARIS MICRO INCISION VACUUM PK 6/BX
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·July 17, 2014
STELLARIS 2EGA VITRECTOMY CUTTER
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·August 1, 2013
STELLARIS POST VITRECTOMY PACK W AFI & FF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·August 1, 2013
STELLARIS POST VITRECTOMY PACK W AFI & FF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·August 1, 2013