BEUDAMED
    4 results · 17ms · 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 Status: Injury ×

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·March 2, 2011

    Single Use Electrosurgical Knife KD-612

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·December 15, 2021

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 13, 2022

    CONFIDENCE SPINAL CMT SYS, 11C

    FDA Adverse Event
    Injury ·DEPUY SPINE INC·Product code NDN·November 3, 2021