BEUDAMED
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    GENTEC®

    FDA UDI
    GENTEC(SHANGHAI)CORPORATION·06970966661932·882VR series suction regulator is a suction reg...

    MALLINCKRODT 7.O ET

    FDA Adverse Event
    Malfunction ·MALLINCKRODT·Product code BTR·June 9, 2006

    AESTIVA 3000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code BSZ·October 9, 2007

    PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code PMP·December 12, 2025

    PROCLAIM PLUS IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·May 17, 2026

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·February 7, 2025

    QUEST

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code OET·June 25, 2009

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·May 11, 2026

    PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·November 19, 2024

    PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·July 23, 2025

    GORE ACUSEAL VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·May 25, 2020

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·February 26, 2025

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·March 14, 2025

    PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·July 11, 2025

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 29, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 29, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 29, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 29, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 30, 2015

    BONE STAPLE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code JDR·November 29, 2017