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

    Peridot-TD Spacer system (The Peridot-TD Intervertebral body fusion system), Anterior cervical interbody fusion - ACIF (The Peridot-TD Anterior Cervical Intervertebral body fusion system)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASAP SINUSCOPE 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BD MAX STAPHSR ASSAY, INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Intervertebral Fusion Device With Bone Graft, Cervical

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

    System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen

    FDA classification
    FDA Class 2 ·System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen

    Nasopharyngoscope (Flexible Or Rigid)

    FDA classification
    FDA Class 2 ·Nasopharyngoscope (Flexible Or Rigid)