BEUDAMED
    5,924 results · 147ms · Sources: EU EUDAMED, US FDA

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·ACS MULTI-LINK RX/OTW ULTRA CORONARY STENT SYSTEM

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

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS H115 AND H119 CONTAK CD 2 (CRT-D) CARDIAC RESYNCHRONIZATION THERAPY DEFIBRILLATOR SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·ALLEGRETTO WAVE EYE-Q LASER SYSTEM

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·MULTI LINK RX ZETA CORONARY STENT SYSTEM/ MULTI LINK OTW ZETA CORONARY STENT SYSTEM

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Zenith® Iliac Branch

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·WAVELIGHT ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM

    Implant, Intragastric For Morbid Obesity

    FDA Pre-Market Approval
    FDA Class 3 ·OBALON BALLOON SYSTEM

    Villin [CWWB1] 0.5mL

    FDA registration
    RICHARD-ALLAN SCIENTIFIC LLC·1 product·🇺🇸 United States

    Odyssey Sulcus Cut Guide Size 1

    FDA registration
    STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

    Odyssey Sulcus Cut Guide Size 1

    FDA registration
    STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

    Odyssey Sulcus Cut Guide Size 1

    FDA registration
    Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia

    ManaMed

    FDA UDI
    MANAMED INC·00810113680644·The ManaEZ Rom Elite adjustable knee brace allo...

    ManaMed

    FDA UDI
    MANAMED INC·00810113680668·The ManaEZ Rom Elite adjustable knee brace allo...

    BR06-ARMC

    FDA registration
    L&K BIOMED CO.,LTD.·1 product·🇰🇷 South Korea

    CD8 [SP16] 0.1mL

    FDA registration
    Microgenics Corporation·1 product·🇺🇸 United States

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·SOFLENS (POLYMACON) CONTACT LENSES

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRITY AFX DR MODEL 5346 DUAL CHAMBER PULSE

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

    FDA Pre-Market Approval
    FDA Class 3 ·CONTAK RENEWAL 3 CRT-D MODELS H170/H175, CONTAK RENEWAL 3 HE CRT-D MODELS H177/H179, AND MODEL 2845 VERSION 2.2 SOFTWARE

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·LUMOS DR-T AND LUMOS VR-T

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·PHILOS II DR-T