BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    PROSTHETIC RESTORATION DEVICE

    FDA 510(k)
    FDA Class 1 ·Dental

    QM2/QM300 CONTROL B PACK

    FDA 510(k)
    FDA Class 2 ·Immunology

    ASPIRATING AND IRRIGATING CYSTS NEEDLES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    RECIPROC BLUE FILES, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·December 5, 2025

    RECIPROC BLUE, 4X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·December 23, 2025

    GALILEO ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·January 3, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 8, 2010

    LIGACLIP MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 25, 2014