BEUDAMED
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    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Essure System for Permanent Birth Control

    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

    FDA Pre-Market Approval
    FDA Class 2 ·CILCO ND:YAG LASER

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·CONCEPTUS ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·ESSURE SYSTEM

    Transcervical Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·ESSURE SYSTEM

    Shorts, Standard Lightweight, 2XS

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Lifeward CA, Inc.·1 device

    Shorts, Standard Lightweight, 3XS

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Lifeward CA, Inc.·1 device

    MAGBODY DT-1200, DT-1200T, DT-1200M, DT-1200PT, DT-1200PM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MAGBODY DT-600

    FDA 510(k)
    FDA Class 2 ·Neurology

    FREE ARM(TM)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Autismikysely

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·HUS-yhtymä·1 device

    Omapolku

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·HUS-yhtymä·2 devices

    Lens, Contact (Rigid Gas Permeable), Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·Paragon HDS® (paflufocon B), FluoroPerm® 151 (paflufocon D), Paragon HDS® 100 (paflufocon D) Rigid Gas Permeable Contac