BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    ARIX HAND LOCKING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PEDICLE SCREW MONOAXIAL SCREW 5X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·September 10, 2019

    CUFFLINK(TM) KNOTLESS ANCHOR WITH INSERTER, 4.5MM/5.5MM - PEEK ONLY, CUFFLINK SP(TM) KNOTLESS ANCHOR WITH INSERTER, 4.5

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MULTIFLEX TINNITUS TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PRECISION NOVI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 21, 2020

    SYRINGE 3ML W/SND

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·December 1, 2017

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 1, 2014

    VITROS CHEMISTRY PRODUCTS PHYT SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DIP·May 29, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code NKB·June 17, 2011

    MUST PEDICLE SCREW 8X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2017

    PEDICLE SCREW PEDICLE SCREW 7X45 (2 PCS)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWP·July 4, 2018