BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Jmoon Conductive Gel

    FDA 510(k)
    FDA Class 2 ·Neurology

    Cascadia™ Interbody System

    FDA UDI
    VB Spine LLC·10888857369887·Trial, Size 12x14X13 mm, 20°

    Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Arthrex Distal Radius System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 6, 2025

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 19, 2025

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014

    MEDSTREAM PROGRAMMABLE INFUSION PUMP 20ML

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF - RAYNHAM·Product code LKK·September 12, 2011

    EZ STEER? NAV DS BI-DIRECTIONAL ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·July 23, 2013