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

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    AtriClip FLEX-Mini LAA Exclusion System (ACHM)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VK Couture

    FDA UDI
    Diversified Products, Inc.·00842894183007·

    MODULAR FLEXIBLE REAMER HEAD, Ø12.5mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665000924·

    Advantage ALIF Trial Cage

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215068103·

    Brisbane ALIF Cage

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215018566·

    TRANBERG Thermoguide Therapy System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Neuroblade System

    FDA 510(k)
    FDA Class 2 ·Neurology

    CLINITEK STATUS+

    FDA Adverse Event
    SIEMENS HEALTHCARE DIAGNOSTICS·Product code JIL·May 16, 2016

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·January 8, 2024

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE.LTD.·Product code FRN·November 19, 2008

    LIBERTÉ (TM)

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·September 6, 2011

    LAT CLAW CONNECTOR 45/55MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·July 18, 2013

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 31, 2018

    PRECISE PRO RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIM·December 6, 2012