BEUDAMED
    6 results · 21ms · 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.

    OPUS ESTRADIOL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SPINESELECT POLYSCREW PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XISCAN 4000 TRANSPORTABLE IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·January 29, 2013

    REPROCESSED ETHICON 5MM TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 14, 2010

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 14, 2014