BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    MERIVAARA EMERGENCY PATIENT TROLLEY #436

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Brasseler

    FDA UDI
    Provision·B504OMKM715560·

    NON-BR2000 LARGE BONE BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919095415·KM71-556

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 1, 2012

    SOMNOSCREEN EEG10-20

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    K2M Navigation Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    HAKIM PROG VALVE INLINE SIPHONGUARD

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·June 13, 2014

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·October 15, 2010

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 13, 2012

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021