23 results · 33ms · Sources: EU EUDAMED, US FDA

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VISULAS YAG III

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ETEST LINEZOLID

FDA 510(k)
FDA Class 2 ·Microbiology

VAMOS ANESTHETIC GAS MONITOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

MATRIX DETACHABLE COILS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·October 12, 2010

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code HCG·October 13, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·November 3, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·November 3, 2009

GUGLIELMI DETACHABLE COIL (GDC)

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·November 2, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION BOSTON SCIENTIFIC CORP.·Product code HCG·September 17, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·September 17, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·September 17, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·September 17, 2009

GDC-10 360 DEGREE COIL SR; GDC-10 360 DEGREE SOFT COIL SR; GDC-18 360 DEGREE COI

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIV. BOSTON SCIENTIFIC CORP·Product code HCG·November 11, 2009

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP.·Product code HCG·September 16, 2009

GDC-10 360 DEGREE COIL SR; GDC-10 360 DEGREE SOFT COIL SR; GDC-18 360 DEGREE COI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code HCG·July 20, 2010

GDC DETACHABLE COIL

FDA Adverse Event
Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code HCG·September 17, 2009

ACCU-CHEK ® RAPID-D INFUSION SET

FDA Adverse Event
Injury ·FRESENIUS KABI DEUTSCHLAND GMBH·Product code FPA·April 9, 2013

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·April 6, 2011

INSIGNIA ULTRA

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Injury ·STRYKER NEUROVASCULAR CORK·Product code HCG·September 26, 2013