BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    CLEAN CUFF BLOOD PRESSURE CUFF LINER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LASER FIBEROPTIC DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BLADE PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·VYGON·Product code FOS·February 17, 2021

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 22, 2013

    IDENTITY XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. CRMD·Product code LWP·January 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010