BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    IL PHENOBARBITAL ASSAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909103552·REVELATION DIAMOND 837-012C - 5 PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112281·SURG-I-BAND GREY

    VENX REVOLUTION

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Precision Casting Solutions Total Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THIN OSTEOTOME HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWM·March 26, 2020

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 4, 2017

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 18, 2010

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code DTB·July 2, 2014

    REVISION MOD. STEM Ø24MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·October 21, 2022