BEUDAMED
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    HOFF PASS-LONG

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code GYK·May 15, 2014

    CODMAN BACTISEAL VENTRICULAR CATHETER

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GYK·May 12, 2014

    TUNNELER 600MM RIGID

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO KG·Product code GYK·December 1, 2025

    SHEATH, PERITONEAL INTRODUCER, 46CM - BOX OF 5

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code GYK·May 27, 2020

    POLARIS ADJUSTABLE PRESSURE VALVE SHUNT

    FDA Adverse Event
    Other ·SOPHYSA·Product code GYK·December 30, 2005

    CATHETER PASSER, DISPOSABLE, 38 CM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code GYK·March 24, 2017

    12.5 FR (4.2 MM) (.166 IN.) PEEL-AWAY CATHETER INTRODUCER

    FDA Adverse Event
    Injury ·RAYNHAM·Product code GYK·September 15, 2022

    CATHETER PASSER 60CM

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code GYK·January 19, 2016

    SHUNT TUNNELER

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES IMPLANTS SA·Product code GYK·August 14, 2012

    SHUNT TUNNELER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS SA·Product code GYK·August 14, 2012

    PERITONEAL INTRODUCER SHEATHS 70CM

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCICENCS IMPLANTS SA·Product code GYK·September 29, 2016

    CODMAN

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES PRODUCTION CORPORATION·Product code GYK·August 26, 2022

    SHUNT TUNNELER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code GYK·December 20, 2013

    SHUNT TUNNELER

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCICENCS IMPLANTS SA·Product code GYK·March 25, 2022

    SHUNT TUNNELER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCICENCS IMPLANTS SA·Product code GYK·March 3, 2022

    Integra Peritoneal Introducer Sheaths, 61 cm;Integra NeuroSciences/REF 901-124; Manufacturer Integra NeuroSciences Implants S.A., 2905 Route Des Dolines, 06921 SOPHIA ANTIPOLIS Cedex, France; Distributed by Integra NeuroSciences, 311 Enterprise Drive, Plainsboro, NJ 08536, USA Designed to be used with a Peritoneal Introducer of appropriate length during the placement of a peritoneal drainage catheter in the treatment of hydrocephalus. Designed to be used with a Peritoneal Introducer of appropriate length during the placement of a peritoneal drainage catheter in the treatment of hydrocephalus.

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code GYK·December 22, 2010

    Instrument, Shunt System Implantation

    FDA classification
    FDA Class 1 ·Instrument, Shunt System Implantation

    GVK CORPORATION

    FDA registration
    GVK CORPORATION·1 product·🇺🇸 United States

    1MED

    FDA UDI
    Qyk Brands LLC·00850039859465·1MED Surgical Mask, Level 2, Earloop style non-...

    1MED

    FDA UDI
    Qyk Brands LLC·10850027748846·1MED Disposable Surgical Gown, Large, sterile