BEUDAMED
    10 results · 27ms · 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.

    Ascent 3D

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028451·PESSARY, GELLHORN #7, 3.25"

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·October 30, 2019

    MEDI-THERM HYPER/HYPOTHERMIA SYSTEM, MODELS MTA6900, MTA7900

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICROSCAN DRIED GRAM NEGATIVE MIC/COMBO PANELS AMOXICILLIN/K. CLAVULANATE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LEEP SYSTEM 1000 WORKSTN

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·December 20, 2019

    GOOSE NECK? MICRO SNARE

    FDA Adverse Event
    Injury ·EV3 INC.·Product code DXE·June 6, 2013

    STEALTHSTATON S7 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·June 22, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

    TORNIER PERFORM ANATOMIC AUG MED RIGHT GLENOID 15 DG

    FDA Adverse Event
    Injury ·TORNIER INC·Product code KWS·March 8, 2024