BEUDAMED
    7 results · 19ms · 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.

    ADAC MODEL ARC-5000, GAMMA CAMERA

    FDA 510(k)
    FDA Class 2 ·Radiology

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228730751·GC Initial™ AL Translucent Mod. TM-02, 20g

    FRIALIT PLUS, XIVE S PLUS, XIVE TG PLUS, ANKYLOS PLUS, DENTAL IMPLANT SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Dental

    ZyMot ICSI Sperm Separation Device, ZyMot Multi Sperm Separation Device (850µl, 3ml)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 13, 2014

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·December 13, 2012

    PUMP MMT-722LNAB PRDGM INS BL EN ML

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·October 15, 2010