BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    EXACTECH ACUMATCH INTEGRATED HIP SYSTEM A-SERIES POROUS COATED ACETABULAR COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993082·anteriors; shade A3; mould ITL

    BI-TEMP TEMPERATURE MONITOR,MODEL TM-300D

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Fountain ValveTip Infusion Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·February 8, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014