BEUDAMED
    55 results · 17ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·JUVEDERM HYALURONATE GEL IMPLANTS

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·JUVEDERM HYALURONATE GEL IMPKANTS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·PG ESSENTIO SR SL WW, PG ESSENTIO DR SL WW, PG ESSENTIO DR EL WW, PG PROPONENT SR SL US, PG PROPONENT DR SL US, PG PROPO

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·CYBERTACH

    Prosthesis, Posterior Spinal Elements

    FDA Pre-Market Approval
    FDA Class 3 ·TOPS™ System

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH II MODELS 262-16

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH & INTERTACH II PULSE GENERATORS

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·TELECTRONICS PASAR MODEL 4171 PG

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·CYBERTACH PULSE GENERATOR SYSTEM

    Prosthesis, Posterior Spinal Elements

    FDA Pre-Market Approval
    FDA Class 3 ·TOPS™ System

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH TM IMPLANTABLE PACEMAKER PULSE

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R) FAMILY OF PULSE GENERATORS

    Prosthesis, Posterior Spinal Elements

    FDA Pre-Market Approval
    FDA Class 3 ·TOPS™ System

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH TM IMPLANTABLE PACEMAKER PULSE

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH II MODELS 262-16

    Prosthesis, Posterior Spinal Elements

    FDA Pre-Market Approval
    FDA Class 3 ·TOPS™ System

    Prosthesis, Posterior Spinal Elements

    FDA Pre-Market Approval
    FDA Class 3 ·TOPS™ System