BEUDAMED
    4,599 results · 43ms · Sources: EU EUDAMED, US FDA

    Hys. 027.30.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 040.15.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 029.15.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 027.15.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 050.00.2080

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 040.00.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 029.00.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    Hys. 027.00.3020a

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

    System, Hemodynamic, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·Cordella Pulmonary Artery Sensor System (CorPASS)

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Aurora EV-ICD System

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

    FDA Pre-Market Approval
    FDA Class 3 ·PulseSelect™ Pulsed Field Ablation (PFA) system

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·Quadra Assura/Unify Assura Family of CRt-Ds

    Transcatheter Septal Occluder

    FDA Pre-Market Approval
    FDA Class 3 ·GORE CARDIOFORM Septal Occluder (GSO)

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

    FDA Pre-Market Approval
    FDA Class 3 ·ANTHEM AND FRONTIER II CRT-P'S

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·SYNERGY Everolimus-Eluting Platinum Chromium Coronary Stent System

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Ellipse/Fortify Assura Family of ICDs

    Pulse-Generator, Single Chamber, Sensor Driven, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·MICRONY PACEMAKERS

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·ACCENT, IDENTITY, VERITY, VICTORY AND ZEPHYR PACEMAKERS

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Aorfix AAA Flexible Stent Graft System with Aorflex Delivery Device

    Tissue Adhesive Internal Use

    FDA Pre-Market Approval
    FDA Class 3 ·LIQUIFIX FIX8 Laparoscopic Hernia Mesh Fixation Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device