BEUDAMED
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    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·July 26, 2024

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·October 6, 2022

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·July 15, 2020

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·February 9, 2023

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·December 6, 2024

    DELTA XTEND

    FDA UDI
    DEPUY (IRELAND)·10603295502647·DELTA XTEND Lateralized Glenosphere +6mm Eccent...

    DELTA XTEND

    FDA UDI
    DEPUY (IRELAND)·10603295502623·DELTA XTEND Lateralized Glenosphere +6mm Standa...

    DELTA XTEND

    FDA UDI
    DEPUY (IRELAND)·10603295502630·DELTA XTEND Lateralized Glenosphere +6mm Eccent...

    DELTA XTEND

    FDA UDI
    DEPUY (IRELAND)·10603295502616·DELTA XTEND Lateralized Glenosphere +6mm Standa...

    IBA PROTON THERAPY SYSTEM, MODEL PROTEUS 235

    FDA 510(k)
    FDA Class 2 ·Radiology

    OXINIUM FEMORAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·May 24, 2013

    ELLIPSE DR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·September 30, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 27, 2023

    DENALI JUGULAR SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 21, 2023

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 10, 2023

    SLEEK OTW PTA CATHETER

    FDA Adverse Event
    Injury ·CLEARSTREAM TECHNOLOGIES LTD.·Product code DQY·December 13, 2023

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 6, 2023