BEUDAMED
    1,908 results · 41ms · Sources: EU EUDAMED, US FDA

    cFactor

    Device
    EU MDD · Eu Md Class 2a ·Active Optical Systems Ltd·On the market·12 countries

    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

    FDA Pre-Market Approval
    FDA Class 2 ·NEODYMIUM-YAG OP LASER OPL-3

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

    FDA Pre-Market Approval
    FDA Class 2 ·NEODYMIUM-YAG OP LASER OPL-3

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Anular Closure Device

    Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia

    FDA Pre-Market Approval
    FDA Class 3 ·Optilume™ BPH Catheter System

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Anular Closure Device (ACD)

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device - Model Number BAR-A8-8MM (2730815-A&), Barricaid® Annular Closure Device - Model Numb

    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

    FDA Pre-Market Approval
    FDA Class 2 ·NEODYMIUM-YAG OP LASER OPL-3

    Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia

    FDA Pre-Market Approval
    FDA Class 3 ·Optilume™ BPH Catheter System

    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

    FDA Pre-Market Approval
    FDA Class 2 ·CILCO ND:YAG LASER

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·BARRICAID ANULAR CLOSURE DEVICE (ACD)

    Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia

    FDA Pre-Market Approval
    FDA Class 3 ·Optilume™ BPH Catheter System

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Anular Closure Device

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·Sentus ProMRI OTW QP S-75, 85, 95, L-75, 85, 95, Sentus ProMRI OTW QP S-75/49, 85/49, 95/49, L-75/49, 85/49, 9/49 and Se

    ENDOCAM

    FDA UDI
    Richard Wolf GmbH·04055207013168·LOGIC HD CAMERA CONTROLLER touch screen, color...

    DLP®

    FDA UDI
    MEDTRONIC, INC.·20643169880959·PRESSURE DISPLAY SET W/STOPCOCK 45 INCH