BEUDAMED
    3 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 FDA Adverse Event ×

    ARCHITECT IPTH ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code CEW·June 6, 2014

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 3, 2012

    BLPRT PLUS 5MM-12MM TRC W/ FOAMGRP

    FDA Adverse Event
    Malfunction ·USSC PUERTO RICO·Product code GDH·September 29, 2010