BEUDAMED
    7 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEARTLIGHT

    FDA Adverse Event
    Injury ·CARDIOFOCUS·Product code OAE·November 26, 2018

    CARTIVA

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·July 21, 2020

    G-ARMOR COVERED STENT

    FDA Adverse Event
    Malfunction ·NUMED, INC.·Product code PNF·January 17, 2023

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 24, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    RSVR MMT-326A 10PK PRDGM 1.8ML 13L

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FMF·August 27, 2008

    CARTIVA DEVICE 10MM T20-0329

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·April 23, 2021