BEUDAMED
    43 results · 135ms · Sources: EU EUDAMED, US FDA

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    BEAR Medic Corporation

    Manufacturer
    🇯🇵 Japan

    BEAR MEDIC CORPORATION

    FDA registration
    BEAR MEDIC CORPORATION·2 products·🇯🇵 Japan

    BEAR MEDICAL/BIRD PRODUCTS CORPORATION

    FDA Adverse Event
    Other ·BEAR MEDICAL SYSTEMS, INC.·Product code CBK·June 9, 1999

    POWER X1

    FDA Adverse Event
    Injury ·FERNO-WASHINGTON, INC.·Product code FPO·May 12, 2020

    AFFINITY CP CENTRIFUGAL BLOOD PUMP

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code DWE·December 8, 2021

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code PAH·July 13, 2021

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 11, 2022

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 21, 2013

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·June 1, 2022

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·February 18, 2022

    MISAGO RX SELF-EXPANDING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code NIP·August 31, 2016

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code PAH·December 4, 2021

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code PAH·December 4, 2021

    TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee replacement Catalog Number: 5531-G-312-E

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code MBH·April 13, 2023

    TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for knee replacement Catalog Number: 5532-G-413-E

    FDA Recall
    Open, Classified ·Howmedica Osteonics Corp.·Product code MBH·April 13, 2023

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code KMW·April 8, 2024

    WALLFLEX BILIARY RX FULLY-COVERED STENT SYSTEM, MODEL M00570500,M00570510, M0057

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·June 24, 2010

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·September 21, 2016

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·September 21, 2016

    MISAGO RX SELF-EXPANDING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code NIP·August 31, 2016