BEUDAMED
    2,346 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS II/GlideLight catheters

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATHS (SLS)

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS ll/GlideLight Catheters

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS SPECTRANETICS LASER SHEATHS

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·Glidelight Laser Sheath

    Oximeter, Fetal Pulse

    FDA Pre-Market Approval
    FDA Class 3 ·OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS/GlideLight

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATHS SLS

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATH (SLSII)

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS CVX-300 EXCIMER LASER SYSTEM & LASER SHEATH

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATHS (SLS)

    Oximeter, Fetal Pulse

    FDA Pre-Market Approval
    FDA Class 3 ·OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATH (SLS)

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS SPECTRANETICS LASER SHEATHS

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS SPECTRANETICS LASER SHEATHS

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SLS SPECTRECTRANETICS LASER SHEATHS

    COAXIAL BALLOON URETHRAL DILATOR

    FDA 510(k)
    FDA Class 3 ·Unknown

    Replacer, Urethral

    FDA classification
    FDA Class 3 ·Replacer, Urethral

    Immunohistochemistry Assay, Antibody, Programmed Death-Ligand 1

    FDA classification
    FDA Class 3 ·Immunohistochemistry Assay, Antibody, Programmed Death-Ligand 1

    Immunohistochemistry Assay, Antibody, Met

    FDA classification
    FDA Class 3 ·Immunohistochemistry Assay, Antibody, Met