BEUDAMED
    74 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SIGNATURE SE I INFUSION PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·November 21, 2019

    SIGNATURE SE I INFUSION PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·November 20, 2019

    E360 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·March 22, 2016

    REVIVE - THROMBECTOMY DEVICE

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·August 14, 2013

    CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·January 4, 2018

    ADVIA CENTAUR

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code SEI·April 15, 2026

    ATELLICA IM HBC TOTAL 2 (HBCT2)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD.·Product code SEI·March 23, 2026

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·January 20, 2026

    COMPLETE SE STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·May 7, 2010

    COMPLETE SE ILIAC

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIO·January 18, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 8, 2012

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 10, 2014

    NOVUM IQ

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·April 29, 2025

    ABSOLUTE PRO .035 SELF EXPANDING STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code FGE·March 25, 2011

    REVIVE - THROMBECTOMY DEVICE

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code DXE·February 21, 2017

    ARCTIC SUN® 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·April 17, 2023

    REVIVE - THROMBECTOMY DEVICE

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code DXE·April 19, 2017

    INDUCTOS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·February 17, 2026

    REVIVE SE 4.5MM OUS

    FDA Adverse Event
    Malfunction ·REFER TO SECTION H10·Product code DXE·March 2, 2018

    REVIVE SE 4.5MM OUS

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code DXE·September 26, 2019