BEUDAMED
    829 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Catheter, Percutaneous (Valvuloplasty)

    FDA Pre-Market Approval
    FDA Class 3 ·INOUE BALLOON CATHETER

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA DERMAL REGENERATION TEMPLATE

    Catheter, Percutaneous (Valvuloplasty)

    FDA Pre-Market Approval
    FDA Class 3 ·INOUE BALLOON CATHETER

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NEW JERSEY LCS(R) UNICOMPARTMENTAL KNEE

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA DERMAL REGENERATION TEMPLATE

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA DERMAL REGENERATION TEMPLATE - TERMINALLY STERILIZED

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA DERMAL REGENERATION TEMPLATE

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·LCS(R)TOTAL KNEE SYSTEM

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA DERMAL REGENERATION TEMPLATE, INTEGRA MESHED DERMAL REGENERATION TEMPLATE

    Device, Dermal Replacement

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE

    BALL TIP, MODEL #030-188

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    H.N. METAL BACKED ACETABULAR CUP, NONCEMENTED

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    GENERATOR, PULSE, IMPLANTABLE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    WEDGE TIP, SMALL, MODEL #030-191

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    WEDGE TIP, SMALL, MODEL #030-194

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    BALL TIP, MODEL #030-185

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    NOVATHERM

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·Restylane Injectable Gel

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·RESTYLANE® Family of Injectable Gels