BEUDAMED
    5,451 results · 42ms · Sources: EU EUDAMED, US FDA

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus Cochlear Implant Systems

    Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus Hybrid Cochlear Implant

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus Cochlear Implant Systems

    Implant, Auditory Brainstem

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus Auditory Brainstem Implant

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus Cochlear Implant Systems

    Sensor, Glucose, Invasive

    FDA Pre-Market Approval
    FDA Class 3 ·DEXCOM G5 MOBILE CONTIUOUS GLUCOSE MONITORING SYSTEM

    Stimulator, Electrical, Implanted, For Parkinsonian Tremor

    FDA Pre-Market Approval
    FDA Class 3 ·ACTIVA DEPP BRAIN STIMULATION ACTIVA PC, ACTIVA SC, ACTIVA RC, KINETRA

    Stimulator, Electrical, Implanted, For Parkinsonian Tremor

    FDA Pre-Market Approval
    FDA Class 3 ·Liberta RC Deep Brain Stimulation (DBS) and NeuroSphere Digital Health App

    VERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein (CPP) Indicator

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TYPE III DENTAL GOLD ALLOY FOR CROWN & BRIDGE APP.

    FDA 510(k)
    FDA Class 2 ·Dental

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·RADIESSE Injectable Implant

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·RADIESSE Injectable Implant, RADIESSE Hands, and RADIESSE (+) Lidocaine Dermal Filler

    AIM Foam swab

    FDA registration
    HLB Life Science CO., LTD·1 product·🇰🇷 South Korea

    Mini-tip QP type 20ul (with plunger)

    FDA registration
    HLB Life Science CO., LTD·1 product·🇰🇷 South Korea

    DUO CURVE

    FDA registration
    GOODPL INC.·1 product·🇰🇷 South Korea

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·GEM III AT WITH APP DEVICE MODEL 7276 AND SOFTWARE MODEL 9974

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC GEM III AT WITH APP DEVICE MODEL 7276 AND SOFTWARE MODEL9974

    APP-HC-03-XX-00 (Head Controller)

    FDA UDI
    W & H Dentalwerk Bürmoos GmbH·J021303440001·Built-in Component

    reSET® Demo Version (Mobile App, Android)

    FDA UDI
    PEAR THERAPEUTICS, INC.·10851580008217·reSET® Mobile Application running on Android. r...

    reSET® Demo Version (Mobile App, iOS)

    FDA UDI
    PEAR THERAPEUTICS, INC.·10851580008200·reSET® Mobile Application running on iOS. reSET...