BEUDAMED
    4,075 results · 44ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·August 14, 2018

    STACLEAR SYRINGE

    FDA Adverse Event
    Malfunction ·TRIBOFILM RESEARCH, INC.·Product code QLY·July 5, 2022

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·August 23, 2021

    PIPELINE

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code OUT·March 27, 2017

    STERI-GAS, STERI-VAC

    FDA Adverse Event
    Malfunction ·3M·Product code FLI·January 18, 2002

    STERI-GAS 4-100 CARTRIDGE

    FDA Adverse Event
    Malfunction ·3M·Product code FLI·September 19, 2000

    STERI-GAS 4-100

    FDA Adverse Event
    Malfunction ·3M CO.·Product code FLI·September 12, 2000

    STERI-GAS 4-100 CARTRIDGE

    FDA Adverse Event
    Malfunction ·3M CO.·Product code FLI·May 19, 2000

    STERI-GAS 4-100 CARTRIDGE

    FDA Adverse Event
    Malfunction ·3M CO.·Product code FLI·January 21, 2000

    COBAS 8000 C 702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 29, 2019

    ELI

    FDA Adverse Event
    Malfunction ·MORTARA INSTRUMENT, INC.·Product code DPS·April 16, 2025

    BILT3 BILIRUBIN TOTAL GEN.3

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CIG·April 29, 2026

    COBAS 6000 CORE UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 20, 2017

    COBAS 8000 C (701) MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 29, 2019

    PUMP MMT-1781KL 670G MG RPL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 3, 2022

    MICROLAP 2MM INTRODUCER

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code HET·June 7, 2016

    ELI 280

    FDA Adverse Event
    Malfunction ·MORTARA INSTRUMENT, INC.·Product code LOS·October 11, 2017

    ELI 280

    FDA Adverse Event
    Malfunction ·MORTARA INSTRUMENTS INC.·Product code DPS·October 4, 2017

    ELI 380

    FDA Adverse Event
    Malfunction ·WELCH ALLYN, INC.·Product code DPS·September 12, 2024

    ELI 380

    FDA Adverse Event
    Malfunction ·WELCH ALLYN, INC.·Product code DPS·September 26, 2024