BEUDAMED
    4,599 results · 47ms · Sources: EU EUDAMED, US FDA

    Agent, Bulking, Injectable For Gastro-Urology Use

    FDA Pre-Market Approval
    FDA Class 3 ·DEFLUX INJECTABLE GEL

    Biologic Material, Dental

    FDA Pre-Market Approval
    FDA Class 3 ·GEM 21S GROWTH FACTOR ENHANCED MATRIX

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·Cerene Cryotherapy Device

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

    FDA Pre-Market Approval
    FDA Class 3 ·HeartLogic™

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Evera MRI XT DR/VR SureScan, Evera MRI S DR/VR SureScan and Visia AF MRI VR SureScan and Implantable Cardioverter Defibr

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·DePuy Ceramax Ceramic Total Hip System

    Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

    FDA Pre-Market Approval
    FDA Class 3 ·CORMET HIP RESURFACING SYSTEM

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver PTX Drug-Eluting Peripheral Stent

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

    FDA Pre-Market Approval
    FDA Class 3 ·PROMOTE, PROMOTE+. PROMOTE RF, PROMOTE ACCEL, UNIFY, QUICKSITE, QUICKFLEX,

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

    FDA Pre-Market Approval
    FDA Class 3 ·Multicenter Automatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT)

    Clear Guide TipTAG

    FDA UDI
    CLEAR GUIDE MEDICAL, INC.·B201CGTT0·

    Echolight S.p.a.

    FDA UDI
    ECHOLIGHT SPA·08052461860039·

    Echolight S.p.a.

    FDA UDI
    ECHOLIGHT SPA·08052461860022·

    Echolight S.p.a.

    FDA UDI
    ECHOLIGHT SPA·08052461860046·

    Hys. 050.70.3020a

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

    Hys. 040.70.3020a

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

    Hys. 040.30.3020a

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

    Hys. 030.30.3020a

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

    Hys. 029.30.3020a

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