BEUDAMED
    10,000 results · 117ms · Sources: EU EUDAMED, US FDA

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC ICD'S

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS COCHLEAR IMPLANT SYSTEM

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Proclaim SCS IPG

    Stent, Iliac

    FDA Pre-Market Approval
    FDA Class 3 ·Cordis® PALMAZ® Balloon-Expandable Stent

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC SPINAL CORD STIMULATION SYSTEMS

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·STAR S4 IR Excimer Laser

    Dorsal Root Ganglion Stimulator For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Proclaim DRG IPG

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·TECNIS iTEC Preloaded Delivery System

    Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)

    FDA Pre-Market Approval
    FDA Class 3 ·DIASORIN ETI-MAK-2 PLUS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·IPAFLUOROFOCON A AND B

    Stimulator, Electrical, Implanted, For Parkinsonian Tremor

    FDA Pre-Market Approval
    FDA Class 3 ·Infinity DBS IPG

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

    FDA Pre-Market Approval
    FDA Class 3 ·INSYNC II MARQUIS

    Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled

    FDA Pre-Market Approval
    FDA Class 3 ·NATRELLE 410 HIGHLY COHESIVE ANATOMICALLY SHAPED SILICONE-FILLED BREAST IMPLANTS

    Visix

    FDA UDI
    TELEVERE SYSTEMS, LLC·00851800007054·Visix 8.1 software Build 81

    Visix

    FDA UDI
    TELEVERE SYSTEMS, LLC·00851800007047·Visix Pro software version 7.7.15

    Visix

    FDA UDI
    TELEVERE SYSTEMS, LLC·00851800007030·Visix software version 2.3.9

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS 22 CHANNEL COCHLEAR IMPLANT

    Pump, Infusion, Implanted, Programmable

    FDA Pre-Market Approval
    FDA Class 3 ·SYNCHROMED II IMPLANTABLE INFUSION SYSTEM

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 9790C PROGRAMMER AND MODEL 9891 PE SOFTWARE