BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ORTHODONTIC CERAMIC BRACKETS

    FDA 510(k)
    FDA Class 2 ·Dental

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973547·

    IRIDIS OPHTHALMIC PHOTOCOAGULATOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    VIGILEO ARTERIAL PRESSURE CARDIAC OUTPUT / OXIMETRY MONITOR; VIGILEO APCO / OXIMETRY MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WAVEWRITER ALPHA PRIME

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 23, 2024

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·May 21, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    MESA PEDICLE SCREW

    FDA Adverse Event
    Injury ·K2M, INC·Product code MNI·September 5, 2008