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

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    MANUKA FILL

    FDA 510(k)
    FDA Unclassified ·Unknown

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813872·GENUMEDI PRO SILVER SIZE VII

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 28, 2020

    SOFTLASE G2-SURGICAL DIODE LASER SYSTEM

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

    BACK-TEK

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·October 17, 2023

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·May 20, 2013

    MBT CEM KEEL TIB TRAY SZ3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·June 1, 2011

    UNKNOWN PRODUCT - LEFT HIP

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK·Product code JDI·August 15, 2008

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012