BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    SeaSpine WaveForm C Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025

    Richard-Allan® Needle 1/2 Circle Taper

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00840113219643·Intent to be used with suture material for tiss...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707039532·DB BRACKETS 22 H/W 20VS BIC

    STERITEC CONTAINERS SYSTEM & MEDITRAY PRODUCTS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ADVIA 120 HEMATOLOGY SYSTEM, CYANIDE-FREE HIGH DETERMINATION

    FDA 510(k)
    FDA Class 2 ·Hematology

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 29, 2008

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·July 12, 2011

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2013