BEUDAMED
    145 results · 36ms · Sources: EU EUDAMED, US FDA

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    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Globe® Pulsed Field System

    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Globe® Catheter; Globe® Pulsed Field System

    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Globe® Pulsed Field System

    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Globe® Catheter; Globe® Pulsed Field System

    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Globe Catheter (601-01000)

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00887517441027·Universal Bender, Cross Connector Left

    LCP

    FDA UDI
    Synthes GmbH·10886982164599·4.5MM LCP PROXIMAL TIBIA PLATE 12 HOLES/226MM-R...

    Gyrus ACMI

    FDA UDI
    Gyrus ACMI, LLC·00821925031913·PAPARELLA-TYPE VENT TUBE 1.02 MM I.D. SILICONE

    Bernafon

    FDA UDI
    Sbo Hearing A/S·05714464052370·ALPHA 7 FW 1.3.0

    PAPARELLA-TYPE VENT TUBE, SILICONE .040" (6/PK)

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code ETD·December 11, 2019

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036035914·

    PIRANHA

    FDA UDI
    SPINAL ELEMENTS·00840916112318·2-L CERV PLATE-44mm

    Trial BiPolar Head

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215045494·

    CADDIE

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

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024119307·

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·MATRIX VASCULAR CLOSURE SYSTEM (VSG)

    Nitric Oxide Generator And Delivery System

    FDA Pre-Market Approval
    FDA Class 3 ·LungFit PH

    PAPARELLA-TYPE VENT TUBE, SILICONE .040" (6/PK)

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code ETD·December 11, 2019

    20ML DISCARDIT¿ II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 1, 2017

    CELL-DYN WBC REAGENT A

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·November 24, 2008