BEUDAMED
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    Filters Status: Malfunction ×

    RELIZORB

    FDA Adverse Event
    Malfunction ·ALCRESTA THERAPEUTICS, INC.·Product code PLQ·August 28, 2025

    RELIZORB IMMOBILIZED LIPASE CARTRIDGE

    FDA Adverse Event
    Malfunction ·ALCRESTA THERAPEUTICS, INC.·Product code PLQ·August 14, 2024

    RELIZORB

    FDA Adverse Event
    Malfunction ·ALCRESTA THERAPEUTICS, INC.·Product code PLQ·November 19, 2024

    RELIZORB

    FDA Adverse Event
    Malfunction ·ALCRESTA THERAPEUTICS, INC·Product code PLQ·January 8, 2026

    RELIZORB

    FDA Adverse Event
    Malfunction ·ALCRESTA THERAPEUTICS, INC.·Product code PLQ·January 29, 2025

    GLP ALIQUOT MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT AUTOMATION SOLUTIONS GMBH·Product code JQP·August 6, 2025

    DIMENSION VISTA 500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·October 15, 2024

    H/B-11 MPA 7 PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 21, 2008

    FLEXLAB

    FDA Adverse Event
    Malfunction ·INPECO SA·Product code CEM·March 6, 2024

    SPY ELITE DRUG DRAPE KIT (SPY PAQ)

    FDA Adverse Event
    Malfunction ·NOVADAQ TECHNOLOGIES·Product code IZI·April 18, 2019

    PUNHO EM T PEQ C/ENC-HEX

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·July 28, 2022

    VALIANT CAPTIVIA - FF

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·October 22, 2019

    ELI380 ERGO WAM WLAN USB DICOM PDQ IEC B

    FDA Adverse Event
    Malfunction ·MORTARA INSTRUMENT·Product code DPS·November 30, 2020

    SINGLE USE LIGATING DEVICE

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code MND·April 11, 2025

    SINGLE USE LIGATING DEVICE

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code MND·April 11, 2025

    SINGLE USE LIGATING DEVICE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FHN·January 24, 2018

    VALIANT CAPTIVIA - FF

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·October 22, 2019

    SINGLE USE LIGATING DEVICE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FHN·March 27, 2018

    VNUS TUBING KIT X15

    FDA Adverse Event
    Malfunction ·KIMAL PLC·Product code KRA·February 20, 2012

    VNUS TUBING KIT X15

    FDA Adverse Event
    Malfunction ·KIMAL PLC·Product code KRA·January 5, 2012