BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    Stryker OrthoMap Versatile Hip System

    FDA 510(k)
    FDA Class 2 ·Neurology

    BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304254428·

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·December 24, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·September 24, 2021

    OSTEOPHIL BETA-TCP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRANSDISCAL SYSTEM, MODELS TDP-17-150-6, TDI-17-150, TDA-PPU-1, TDA-TBK-1, TDX-Y-TSW-TDP, TDX-PMG-PPU

    FDA 510(k)
    FDA Class 2 ·Neurology

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code LWP·October 10, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·August 10, 2023