BEUDAMED
    10 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 ×

    CEFOPERAZONE 75MCG SENSI-DISC

    FDA 510(k)
    FDA Class 2 ·Microbiology

    STRADIS

    FDA UDI
    STRADIS MEDICAL, LLC·M75268212641·CUSTOM SURGICAL KIT, VEIN PACK

    STRADIS

    FDA UDI
    STRADIS MEDICAL, LLC·M75268212640·CUSTOM SURGICAL KIT, VEIN PACK

    PEDICLE SCREW MUST STRAIGHT CROSS CONNECTOR 20MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWP·September 4, 2019

    TRZ-CG POWER POSITIONING SYSTEM WITH CENTER-OF-GRAVITY SHIFTING POWER TILT, RECLINE, AND POWER ELEVATING SEAT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TRITON ELECTRIC HIGH TORQUE HANDPIECE AND SOFTWARE MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery

    FDA Enforcement
    Class II ·Completed·Stradis Healthcare, LLC.·July 15, 2015

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - HAINA, SAN CRISTOBAL·Product code FPA·May 20, 2014

    8.5MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HTO·November 6, 2012

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 5, 2015