459 results · 21ms · Sources: EU EUDAMED, US FDA

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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

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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