BEUDAMED
    52 results · 29ms · Sources: EU EUDAMED, US FDA

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    REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Copper Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989025507·COPPER NITI 27 BAF 16 DIA L/S PK10

    Altus Spine Pedicle Screw System

    FDA UDI
    Altus Spine, LLC·00843210132006·Rod Rocker

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100460·ASSEMBLY, CADDIE, CURVED RODS WITH STOPS

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420500460·Anterior Lateral Wedge Osteotomy Guide, 50mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410500460·Anterior Closing Wedge Osteotomy Guide, 50mm x ...

    KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NUVOLASE 532 MEDICAL LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE LEAD SYSTEM

    MARY HITCHCOCK HANOVER NH 1

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·November 7, 2012

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·Product code FOZ·September 16, 2021

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE IS-1 LEADS

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE HEART FAILURE LEAD FAMILY

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE LEAD SYSTEM

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE CRTS

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERALE LEADS MODELS: 4554, 4555

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·Acuity Steerable Lead System

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·Acuity Steerable

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·ACUITY STEERABLE LEAD SYSTEM