BEUDAMED
    4 results · 42ms · 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 ×

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    *

    FDA Adverse Event
    MEDTRONIC SOFAMOR DANEK·Product code HXX·December 16, 2010

    KANGAROO EPUMP

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LZH·January 3, 2013

    UNKNOWN DEPUY PATELLAR COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 14, 2014