BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    CoreHip® System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741722350·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674172235060·

    n/a

    FDA UDI
    Ortho Development Corporation·00822409107599·Deeper Tibial Half Cone Broach Size 35mm

    PM-50 PULSE OXIMETER AND VS-800 VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MANTIS SPINAL SYSTEM & MANTIS REDUX SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNIVERSAL HANDSWITCH

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code EIA·October 15, 2014

    UNIVERSAL MODULAR ELECTRIC/BATTERY DOUBLE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A.·Product code GFA·June 5, 2013

    UNKNOWN M2A PRODUCT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 22, 2011