BEUDAMED
    4 results · 10ms · Sources: EU EUDAMED, US FDA

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    Filters Classification: FDA Class 2 ×

    Rampart One Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Single-Use Internal Condom

    FDA Pre-Market Approval
    FDA Class 2 ·FC2 FEMALE CONDOM

    Single-Use Internal Condom

    FDA Pre-Market Approval
    FDA Class 2 ·FC2 FEMALE CONDOM

    Single-Use Internal Condom

    FDA Pre-Market Approval
    FDA Class 2 ·FC2 FEMALE CONDOM