37 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PHFW-10
FDA 510(k)
FDA Class 2
·Physical Medicine
OBC-096 BREAST ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
VERASTEP
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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
UNKNOWN VERSASTEP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GCJ·June 11, 2015
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
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225398716312717201·RITE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225398716315917201·RITE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022539871632517201·RITE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225398716338117201·RITE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0225398716312017201·RITE