BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm

    FDA 510(k)
    FDA Class 2 ·Dental

    SOLID CANCELLOUS LAG SCREW

    FDA UDI
    Biomet Orthopedics, LLC·00887868005084·

    MODIFICATION TO: ENSEAL PTC TISSUE SEALING DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    FOCUS (TM) ECHOGENIC NERVE STIMULATING NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·October 14, 2014

    CURETTE II T-TIP

    FDA Adverse Event
    Malfunction ·KYPHON NEUCHATEL·Product code LXH·June 16, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·October 4, 2024

    PEDICLE SCREW MUST COMBINED SETSCREW H4-T27 - (4X)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·October 9, 2019

    PEDICLE SCREW 6X45

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWP·July 5, 2019