BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    EARP Nerve Cuff Electrode

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

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707040606·DB BRACKETS 22 H/W T-22 BH 2nd BIC L/L

    UNICON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PLASIATEK ACTUATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VDW SILVER RECIPROCATING MOTOR

    FDA Adverse Event
    Malfunction ·DENTSPLY VDW GMBH·Product code EBW·November 15, 2019

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·September 9, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 10, 2014

    2520274-2013-04576

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 22, 2013

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026