BEUDAMED
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    STOP & GUIDE® KIT

    FDA UDI
    BIOTECHNOLOGY INSTITUTE SL·08435389825449·

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 4, 2026

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KCG·May 12, 2014

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER TRAY

    FDA Adverse Event
    Injury ·COOK INC·Product code KCG·June 10, 2010

    ADVANCE 18 LP LOW PROFILE BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code KCG·June 4, 2010

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KCG·May 12, 2014

    CIAGLIA BLUE DOLPHIN PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KCG·April 11, 2012

    PILLING /WECK/ TELEFLEX

    FDA Adverse Event
    Death ·TELEFLEX MEDICAL·Product code KCG·December 9, 2008

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KCG·April 14, 2009

    CIAGLIA BLUE RHINO G2

    FDA Adverse Event
    Malfunction ·COOK MEDICAL LL·Product code KCG·December 17, 2018

    PILLING/WECK/TELEFLEX

    FDA Adverse Event
    Death ·TELEFLEX MEDICAL·Product code KCG·December 12, 2008

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET

    FDA Adverse Event
    Death ·COOK, INC.·Product code KCG·January 20, 2011

    MIC-KEY* G-20 LAPAROSCOPIC INTRODUCER KIT

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH·Product code KCG·January 3, 2017

    CRE BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORK LTD·Product code KCG·October 26, 2007

    CIAGLIA BLUE RHINO INTRODUCER TRAY

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KCG·June 18, 2004

    PORTEX® ULTRAPERC® SINGLE STAGE DILATOR TECHNIQUE KITS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD; INC.·Product code KCG·September 28, 2018

    TRANSTRACHEAL SYSTEMS

    FDA Adverse Event
    Malfunction ·TRANSTRACHEAL SYSTEMS·Product code KCG·September 15, 1999

    1820334-2021-00885

    FDA Adverse Event
    Injury ·COOK INC·Product code KCG·March 4, 2021

    DIGESTHEALTH ENTERAL FEED DEVICE TUBE KITS

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH·Product code KCG·May 16, 2016

    PORTEX ULTRAPERC DILATOR KIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KCG·February 17, 2022