BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Anatomical Plating System (various)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RS-4I MUSCLE STIMULATOR FAMILY

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VIA MICROCATHETER, VIA PLUS MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code KDW·February 17, 2020

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·September 12, 2014

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 2, 2011

    2520274-2013-04470

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HXX·July 18, 2013

    KIDS OXYGENATOR D101

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 4, 2025