BEUDAMED
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    FDA UDI
    TELEFLEX INCORPORATED·10801902171150·Pressure Injectable Arrowg+ard Blue Plus(R) Thr...

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    FDA UDI
    TELEFLEX INCORPORATED·10801902144123·Pressure Injectable Arrowg+ard Blue Plus(R) Thr...

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    FDA UDI
    TELEFLEX INCORPORATED·10801902171020·Pressure Injectable Arrowg+ard Blue Plus(R) Thr...

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    FDA UDI
    TELEFLEX INCORPORATED·10801902144116·Pressure Injectable Arrowg+ard Blue Plus(R) Thr...

    ARCTIC SUN® 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·November 30, 2022

    VersaCross RF Wire

    FDA UDI
    BOSTON SCIENTIFIC CORPORATION·00685447011095·1 x VersaCross RF Wire; 1 x Connector Cable (Si...

    VersaCross RF Wire

    FDA UDI
    BOSTON SCIENTIFIC CORPORATION·00685447011118·1 x VersaCross RF Wire; 1 x Connector Cable (Si...

    INTELLIVUE MX40 WLAN

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code DSI·August 7, 2023

    INTELLIVUE INFO CENTER IX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 7, 2023

    DATASCOPE INTRA-AORTIC PUMP

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·May 15, 2014

    GYRUS, PK-SP GENERATOR

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code GEI·April 18, 2024

    PERSEUS A500

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code BSZ·February 4, 2022

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 8, 2025

    HIGH FREQUENCY OSCILLATORY VENTILATOR

    FDA Adverse Event
    Malfunction ·SENSORMEDICS, SUBSIDIARY OF THERMO ELECTRON·Product code LSZ·November 21, 1996

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·April 28, 2023

    INTELLIVUE MX40 2.4GHZ

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·March 15, 2023

    3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV)

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code LSZ·July 22, 2016

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 17, 2025

    MX40 1.4 GHZ SMART HOPPING

    FDA Adverse Event
    Death ·PHILIPS NORTH AMERICA LLC·Product code DSI·April 5, 2021

    INTELLIVUE INFORMATION CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 20, 2017