BEUDAMED
    7 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    MARINR SERIES EP DIAGNOSTI CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MIS Spine Frame Instrument Case

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KIMBERLY-CLARK* STERLING* NITRILE POWDER-FREE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GLIDEPATH

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code MSD·May 6, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 9, 2013

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 22, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 6, 2011