BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    SHAWNEE PRODUCTS KIT I

    FDA 510(k)
    FDA Not Classified ·Unknown

    BCLEAR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CARDIAC VX

    FDA 510(k)
    FDA Class 2 ·Radiology

    BASIS¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 29, 2024

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 14, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 13, 2010

    INCEPTA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2014

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024