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

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ST. JUDE MEDICAL

FDA Adverse Event
Other ·ST. JUDE MEDICAL, INC.·Product code LWQ·October 9, 2003

ST JUDE MEDICAL

FDA Adverse Event
Other ·CARDIAC ASSIST DIV. ST. JUDE MEDICAL·Product code DSP·January 31, 1994

ST JUDE MEDICAL

FDA Adverse Event
Other ·ST JUDE MEDICAL·Product code LWS·April 11, 2007

ST. JUDE MEDICAL

FDA Adverse Event
Other ·ST. JUDE MEDICAL INC.·Product code LWQ·February 14, 2001

ST JUDE MEDICAL

FDA Adverse Event
Other ·ST JUDE MEDICAL·Product code LGW·December 11, 2012

ST JUDE MEDICAL

FDA Adverse Event
Other ·Product code DTB·August 23, 2007

ST. JUDE MEDICAL

FDA Adverse Event
Other ·Product code DTB·August 23, 2007

ST. JUDE MEDICAL

FDA Adverse Event
Other ·ST. JUDE MEDICAL·Product code LWQ·August 16, 2005

ST JUDE MEDICAL

FDA Adverse Event
Other ·ST JUDE MEDICAL·Product code DXY·April 22, 2002

ST JUDE MEDICAL

FDA Adverse Event
Other ·ST JUDE MEDICAL·Product code FCP·April 10, 2002

ST. JUDE MEDICAL

FDA Adverse Event
Other ·ST. JUDE MEDICAL, INC.·Product code LWQ·August 22, 2006

ST. JUDE MEDICAL PACEMAKER

FDA Adverse Event
Other ·ST. JUDE CLINICAL STUDIES·Product code DXY·June 15, 2007

ST JUDE MEDICAL LEAD

FDA Adverse Event
Other ·ST. JUDE MEDICAL, INC.·Product code DTB·April 23, 2008

ST JUDE MEDICAL, ICD DEVICE

FDA Adverse Event
Other ·ST. JUDE MEDICAL, INC.·Product code LWS·June 22, 2010

ST. JUDE MEDICAL DEFIBRILLATION LEAD

FDA Adverse Event
Other ·ST. JUDE MEDICAL·Product code LWS·July 12, 2012

LUMAX 540 VR-T

FDA Adverse Event
Other ·BIOTRONIK SE &CO. KG·Product code MRM·June 13, 2011

PHILOS DR

FDA Adverse Event
Other ·BIOTRONIK GMBH & CO.·Product code DXY·November 2, 2005

STANDARD CUFF

FDA Adverse Event
Other ·ST. JUDE MEDICAL PUERTO RICO, INC.·Product code LWQ·July 16, 1997

DAIG CORP. ST. JUDE MEDICAL CO.

FDA Adverse Event
Other ·DAIG CORP.·Product code DYB·January 25, 1999

SWARTZ 8.5F BRAIDED TRANS INTRODUCER, SL0, 63CM

FDA Adverse Event
Other ·ST. JUDE MEDICAL, AF DIVISION·Product code DYB·November 4, 2009