BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    PUNCTUAL OCCLUDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970631·anteriors; shade A3 light; mould UBXL

    DEVICE MODIFICATION TO RADIUS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLEX ARM BE 122, CLAMP 122-27

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    43 CM (17") APPX 6.9 ML, TRIFUSE ADD-ON SET W/3 CLAMPS (BLUE, 2 RED), DRY SPIKE

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·May 23, 2023

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·June 2, 2014

    PROXIMATE

    FDA Adverse Event
    ETHICON ENDO-SURGERY, INC.·Product code GDW·May 18, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013