BEUDAMED
    8 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.

    SAF-D-FIB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209109272·KIT, M-FAK - ODG - CUSTOM

    GLUCOPACK

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACUSON NX3 Elite / NX3 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    WAVEONE GOLD PRIMARY 3-FILE STER 25MM

    FDA Adverse Event
    Malfunction ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EKS·August 20, 2024

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·June 5, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 13, 2012

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 29, 2010