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

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    Filters Regulation: Us FDA ×

    LineSider® Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139233210·Unity ASC Tibial Insert Trials Size 7 to 9 9-14...

    BD BBL™ Taxo™ Differentiation Discs for Sucrose

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902310983·BD BBL™ Taxo™ Differentiation Discs for Sucrose

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116022748·Dornier 400 µm Single-Use ND YAG Laser Fiber 3.5m

    EMERGENCY PORTABLE VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    3-CCD DIGITAL CAMERA 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

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·November 19, 2020

    PLUM A+ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 30, 2008

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 1, 2011

    PLUM A+ DRIVER EDITI

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·July 12, 2013