BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010

    PFNA-II BLADE L85 TAN

    FDA Adverse Event
    Injury ·SYNTHES·Product code HSB·December 3, 2012

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 18, 2015

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·November 2, 2020

    ATTAIN PERFORMA S MRI SURESCAN

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code OJX·November 2, 2020

    SPRINT QUATTRO SECURE MRI SURESCAN

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code NVY·November 2, 2020

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·September 17, 2021

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·September 17, 2021

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 13, 2025