BEUDAMED
    10 results · 48ms · Sources: EU EUDAMED, US FDA

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    p-Chip Wand Reader

    FDA Recall
    Open, Classified ·p-Chip Corporation·Product code RFN·March 3, 2021

    p-Chip Wand Reader

    FDA Enforcement
    Class II ·Ongoing·p-Chip Corporation·June 21, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·June 4, 2019

    EVIS LUCERA ELITE COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·December 12, 2022

    OPTIFLUX 180NRE DIALYZER FINISHED ASSY.

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·February 20, 2020

    FLEXIVA (TM) ID TRACTIP HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·December 4, 2018

    FLEXIVA ID TRACTIP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·December 4, 2018

    FLEXIVA (TM) ID TRACTIP HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·November 27, 2018

    FLEXIVA (TM) ID HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·November 28, 2018

    CMC Medical Devices & Drugs SL

    Authorized representative
    🇪🇸 Spain·698 Manufacturers·11260 Devices