BEUDAMED
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    OWENS & MINOR

    FDA Adverse Event
    Malfunction ·OWENS & MINOR DC 74·Product code GDW·February 10, 2012

    HANDFORM-WURZELHEBER 623/74

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code EMJ·June 11, 2021

    #7 4:1 CUTTING BLOCK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·October 5, 2010

    #7 4:1 CUTTING BLOCK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·March 20, 2017

    AXS VECTA 74 INTERMEDIATE CATHETER

    FDA Adverse Event
    Malfunction ·STRYKER CORPORATION·Product code NRY·May 30, 2023

    OX.CAN. 10/210/74 MM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL LTD.·Product code CAT·November 9, 2015

    ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MIH·May 8, 2019

    ELITE 12CM STRAIGHT ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HBE·January 16, 2024

    ELITE 7CM STRAIGHT ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HBE·January 21, 2025

    78/74 A/P L FEMORAL

    FDA Adverse Event
    Malfunction ·DEPUY RAYNHAM / DIV. OF DEPUY ORTHOPAEDICS, INC.·Product code HSA·August 14, 2000

    PTA OPTA 5F 135CM 7#4

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V. (RODEN)·Product code LIT·March 11, 2000

    TRUERESULT

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·September 4, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·August 19, 2014

    ZIMMON BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 8, 2024

    ZIMMON BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·July 5, 2022

    ARCTIC SUN® 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·January 22, 2024

    COBAS INTEGRA 400

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 20, 2008

    A19 ALLSET GOLD SSP KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·September 14, 2012

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 28, 2009

    ZIMMON BILIARY STENT SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 17, 2020