BEUDAMED
    409 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·Assurity Pacemaker & Endurity Pacemaker

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PROMUS Element Plus Everolimus-Eluting Plaatinum Chromium Coronary Stent System (Monorail and Over-the-Wire), PROMUS PRE

    Transcatheter Septal Occluder

    FDA Pre-Market Approval
    FDA Class 3 ·GORE® CARDIOFORM ASD Occluder

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·Adapta, Versa, Sensia IPG, Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra XT SR MRI IPG, Attesta DR

    Scaffold, Infrapopliteal, Absorbable

    FDA Pre-Market Approval
    FDA Class 3 ·Esprit™ BTK Everolimus Eluting Resorbable Scaffold System

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·ALTERNATE LASER SOURCE

    Aortic Valve, Prosthesis, Percutaneously Delivered

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC COREVALVE SYSTEM

    Lens, Multifocal Intraocular

    FDA Pre-Market Approval
    FDA Class 3 ·ACRYSOF RESTOR POSTERIOR CHAMBER IOL

    Aid, Surgical, Viscoelastic

    FDA Pre-Market Approval
    FDA Class 3 ·SODIUM HYALURONATE OPHTHALMIC VISCOELASTIC DEVICES

    Ventricular (Assist) Bypass

    FDA Pre-Market Approval
    FDA Class 3 ·EXCOR Connecting and Extension Sets

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·ACCULINK CAROTID STENT SYSTEM

    Mr-Guided Focused Ultrasound System

    FDA Pre-Market Approval
    FDA Class 3 ·Exablate Model 4000 System

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·MULTI-LINK VISION FAMILY OF CORONARY STENT SYSTEMS

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·MULTI-LINK FAMILY OF CORONARY STENT SYSTEMS

    Stimulator, Autonomic Nerve, Implanted (Depression)

    FDA Pre-Market Approval
    FDA Class 3 ·ASPIRESR GENERATOR -MODEL 106

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·AMS 800 Artificial Urinary Sphincter with and without InhibiZone Treatment

    Prosthesis, Penis, Inflatable

    FDA Pre-Market Approval
    FDA Class 3 ·AMS 700 Implantable Penile Prosthesis with and without Inhibizone Treatment

    Ring, Endocapsular

    FDA Pre-Market Approval
    FDA Class 3 ·EYEJET INJECTOR

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·HORIZON(TM) YAG LASER MODEL 2000

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·HORIZON(TM) YAG LASER MODEL 2000