46 results · 64ms · Sources: EU EUDAMED, US FDA

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PETITE PORT-A-CATH, 7 FR

FDA Adverse Event
Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·February 23, 1996

COOK PACEMAKER CORP. 115 UNIPOLAR CARDI

FDA 510(k)
FDA Class 3 ·Cardiovascular

COOK PACEMAKER CORP. 116 BIOPOLAR CARDI

FDA 510(k)

COOK PACEMAKER CORP. 327T, SERIES R UNIPOLAR CARDI

FDA 510(k)
FDA Class 3 ·Cardiovascular

COOK PACEMAKER CORP. 332T BIPOLAR CARDIAC PULSE GE

FDA 510(k)
FDA Class 3 ·Cardiovascular

VITAL PORT VASCULAR ACCESS SYSTEM

FDA Adverse Event
Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·December 28, 1995

BYRD DILATOR SHEATH SET TEFLON

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code GCC·September 23, 1996

VITAL PORT CATHETER

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code DQO·January 12, 1994

VITAL PORT

FDA Adverse Event
Other ·COOK PACEMAKER CORP.·Product code LJT·March 10, 1994

VITAL PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·February 7, 1995

VITAL PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LTH·February 13, 1995

VITAL-PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·February 1, 1995

VITAL PORT ACCESS SYSTEMS

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·January 19, 1995

COOK VITAL PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code DQO·October 26, 1994

VITAL PORT ACCESS DEVICE

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·June 26, 1997

VITAL-PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·November 8, 1996

VITAL-PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·November 13, 1996

VITAL-PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·December 6, 1996

VITAL-PORT

FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·November 13, 1996

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FDA Adverse Event
Injury ·COOK PACEMAKER CORP.·Product code LJT·October 23, 1996