BEUDAMED
    6 results · 18ms · 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.

    HY-TEC/MANUAL AUTOIMMUNE KIT FOR MITOCHONDRIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    MX MOBILE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    KIT MENDEC SPINE AND DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASR 300 SPIKED CUP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 14, 2013

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    BONE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 29, 2014