BEUDAMED
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    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·04250328210414·FUSE PLIF INSERTER TUBE

    Innomed, Inc.

    FDA UDI
    INNOMED, INC.·00840277103796·Stulberg Leg Holder Footpiece Carbon Fiber

    Innomed, Inc.

    FDA UDI
    INNOMED, INC.·00840277104649·Robb Leg Positioner Footpiece Carbon Fiber

    FLEXABILITY ABLATION CATHETER-UNKNOWN

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL, COSTA RICA LTDA·Product code OAD·September 24, 2025

    TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, COSTA RICA LTD·Product code OAE·February 12, 2024

    SI BRITE TIP

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DYB·October 10, 2014

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code FGE·April 8, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·April 22, 2010

    SI AVANTI PLUS

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·February 7, 2011

    SI BRITE TIP

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DYB·March 4, 2011

    TACTIFLEX¿ ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAE·May 10, 2024

    P3-PRONG BEND-PLIERS F/PI 1.5/2

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTC·May 2, 2012

    SI BRITE TIP

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DYB·July 7, 2008

    CCYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·November 14, 2008

    TACTIFLEX¿ ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code OAE·March 17, 2026

    Excursion

    FDA UDI
    BRIVANT LIMITED·00816349011610·

    MINI SHEET

    FDA Adverse Event
    Injury ·ZIMMER SURGICAL·Product code FPY·June 20, 2012

    MEDSOURCE AND CURAPLEX

    FDA Adverse Event
    Malfunction ·Product code FPY·September 30, 2025

    DISPOSABLE BURN SHEET

    FDA Adverse Event
    MATRIX MEDICAL, INC.·Product code FPY·October 6, 1995

    BURN SHEET

    FDA Adverse Event
    Malfunction ·DUKAL CORPORATION·Product code FPY·April 19, 2017