BEUDAMED
    9 results · 37ms · Sources: EU EUDAMED, US FDA

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    EXACTECH ACAPELLA ONE CERVICAL SPACER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNITY NETWORK PATIENT DATA SERVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HAHN TAPERED IMPLANT Ø3.5 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 2, 2024

    FLEXOR RADIAL ACCESS SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DYB·April 13, 2015

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·May 29, 2013

    ARMEDICA HI-LO TREATMENT TABLE

    FDA Adverse Event
    Injury ·ARMEDICA MFG. CORP.·Product code INQ·September 24, 2014

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·June 17, 2011

    FLEXOR RADIAL ACCESS SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·July 12, 2016