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

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    SONGER(TM) CABLE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909137352·REVELATION DIAMOND 879K-018SC - 5 PACK

    HEXIDIS ALCOHOL SWAB

    FDA 510(k)
    FDA Unclassified ·Unknown

    dS Sentinelle Breast 16ch 1.5T Coil

    FDA 510(k)
    FDA Class 2 ·Radiology

    TROJAN PLEASURE PACK LUBRICATED CONDOMS

    FDA Adverse Event
    Injury ·CHURCH & DWIGHT CO., INC.·Product code HIS·October 29, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 14, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·November 12, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 3, 2014

    PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSX·October 15, 2025

    GENESIS UNI KNEE FEMORAL COMPONENT COCR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSX·May 23, 2025