BEUDAMED
    4,050 results · 47ms · Sources: EU EUDAMED, US FDA

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    Strp Insert Only, DFA Plus, A Size, 2.5in

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    Strp Insert Only, DFA Plus, A Size, 2.25in

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    Strp Insert Only, DFA Plus, A Size, Y

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    Strp DFA, Spl, Cal Plate B-Size PR

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    Strp DFA, Spl, Cal Plate A-Size PR

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    Model 6942 Bidirectional Torque Wrench

    FDA registration
    Boston Scientific Corporation·4 products·🇺🇸 United States

    DF1-1069 B BARRES PARALLELES FIXES 5M

    Basic UDI-DI
    EU MDD · Eu Md Class 1 ·ETABLISSEMENTS FRANCO ET FILS·1 device

    Disc-FX® Guidewire

    FDA UDI
    ELLIQUENCE, LLC·00846338010911·

    Disc-FX® Guidewire

    FDA UDI
    ELLIQUENCE, LLC·00846338001476·

    Disc-FX® Guidewire

    FDA UDI
    ELLIQUENCE, LLC·00846338001483·

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CONCERTO ICD, CONCERTO II CRT-D, CONSULTA, CONSULTA DF4, MAXIMO II CRT-D, PROTECTA CRT-D, PROTECTA DF-DF-4, PROTECTA XT

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

    FDA Pre-Market Approval
    FDA Class 3 ·PROTECTA XT/PROTECTA/CONSULTA/MAXIMO II CRT-D DF4

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·IS4/DF4 Connector Sleeve; Suture Sleeve; Suture Sleeve Kit

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

    FDA Pre-Market Approval
    FDA Class 3 ·PROTECTA XT/PROTECTA/CONSULTA/MAXIMO II CRT-D DF4

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Protego SD; Protego TD; Protego DF-1 SD; Protego ProMRI SDx; Protego DF-1; ProMRI SD; Plexa SD; Plexa ProMRI SD; Plexa D

    AJT, DFA, Anodized Alum Upr, 3/16x1/2 Pair

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    AJT, DFA, Adult, 1/8 Slot, LL/RM SlSp

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    AJT, DFA, Adult, 1/8 Slot, LL/RM SlPin

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    AJT, DFA, Adult, 1/8 Slot, LL/RM HPin

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries

    Tamarack DFA Flexure Joint, PED 95 Duro Blk 5PK

    Device
    EU MDR · Eu Md Class 1 ·Becker Orthopedic Appliance Company·On the market·32 countries