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

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    Filters Regulation: Us FDA ×

    ZIMMER NEXEL TOTAL ELBOW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ZIO PATCH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SOLID SCREWDRIVER, SMALL

    FDA Adverse Event
    Malfunction ·CONVENTUS FLOWER ORTHOPEDICS·Product code HXX·August 17, 2021

    SWISS LITHOCLAST

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, CORP·Product code FFK·March 11, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 14, 2011

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·November 25, 2024