BEUDAMED
    3,512 results · 47ms · Sources: EU EUDAMED, US FDA

    Discovery PET CT

    FDA UDI
    GE MEDICAL SYSTEMS, INC.·10840682142875·

    Discovery

    FDA UDI
    GE MEDICAL SYSTEMS, INC.·00840682102995·

    Pacemaker/Icd/Crt Non-Implanted Components

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2202.U and NEO 2202.U

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2100.U and NEO 2100.U

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2100.U and NEO 2100.U

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2100.U and NEO 2100.U

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2100.U and NEO 2100.U

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2100.U and NEO 2100.U

    ATOZ Expander Kit

    FDA UDI
    MK Meditech Inc.·08800197900341·The ATOZ Expander Kit is a procedure kit used f...

    ATOZ Expander Kit

    FDA UDI
    MK Meditech Inc.·08800197900075·ATOZ Expander Kit *10SET

    ATOZ Expander Kit

    FDA UDI
    MK Meditech Inc.·08800197900068·The ATOZ Expander Kit is a procedure kit used f...

    RELAXZEN

    FDA registration
    XIAMEN COMFIER TECHNOLOGY CO., LTD.·1 product·🇨🇳 China

    Pacemaker/Icd/Crt Non-Implanted Components

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    SYSTEMATE PHOSPHORUS TEST TECHNICON RA 1000

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CLINICARD PHOSPHORUS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PHOSPHORUS TEST (PHOS) ITEM #65666

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry