BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    3M 1154 LASER IMAGER

    FDA 510(k)
    FDA Class 2 ·Radiology

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194994·Interbody, 9mm x 36mm x 14mm, 20 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202989·Interbody, 9mm x 36mm x 14mm, 20 deg

    SYNELISA U1-SNRNP (68KDA)-ANTIBODIES

    FDA 510(k)
    FDA Class 2 ·Immunology

    INSTRUMENTS FOR LAPAROSCOPIC USE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MENTOR SMOOTH ROUND HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·June 13, 2018

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 30, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·December 13, 2010

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 15, 2014