BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACE CORTICAL BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450295779·

    REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS

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

    AMERICAN SURGICAL COMPANY/ NEUROSURGICAL SPONGES (BRAND)

    FDA 510(k)
    FDA Class 2 ·Neurology

    TITAN TOUCH INFR ZERO ANG 18CM

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·July 23, 2018

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 13, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-REDWOOD CITY·Product code MGB·December 2, 2010

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NIK·July 3, 2014

    Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025