BEUDAMED
    5 results · 86ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·June 10, 2015

    PRN 50-M+, GE part number 2062759-001, manufacturer part number 600-23310-01 Product Usage: The PRN 50M+ Paper Chart Recorder thermally records patient data on a paper strip. This device is intended for use under direct supervision of a licensed health care practitioner. This device is not intended for home use.

    FDA Recall
    Terminated ·Gsi Group Inc·Product code DSF·December 2, 2015

    EXCIMER LASER

    FDA Adverse Event
    Injury ·UNK·Product code LZS·September 19, 2019

    RADIESSE (+) INJECTABLE IMPLANT

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC·Product code LMH·January 10, 2022

    BIOGLUE - UNKNOWN CONFIGURATION

    FDA Adverse Event
    Injury ·CRYOLIFE, INC. - KENNESAW·Product code MUQ·November 2, 2020