BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    VerteLoc Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93082311340C0·Custom Cobb Elevator 11" 3/4"

    3 MODULE CORE WITH ISE600

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORP.·Product code JJE·April 23, 2007

    DISPOSABLE POWDERED VINYL EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Arthrex NanoScope System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 20, 2025

    PLUMSET-DUAL W/CON PP, CAP PORT & CLAVE

    FDA Adverse Event
    Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FPA·October 30, 2008

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 26, 2011

    RENEGADE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code KRA·June 26, 2013