BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    4.0 and 6.5 Cancellous Bone Screw and Washer

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CZ-S2000

    FDA 510(k)
    FDA Class 2 ·Dental

    INTRAVSCULAR ADMINISTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENTRUST

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·October 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    RA600

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code LLZ·June 16, 2011

    LOGIC TIBIAL KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 13, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWI·August 14, 2024