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

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    AAP CANNULATED SCREW, 7.5MM, 4.5MM, 4.0MM, 3.5MM, 7.0MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DADE LOW IONIC STRENGTH SOLUITION (LISS)

    FDA 510(k)
    FDA Class 2 ·Hematology

    MEGAPULSE LASER SYSTEM AND FIBERS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·November 5, 2024

    ALINITY I CEA REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code DHX·May 18, 2026

    V 2.0 FIRM EXT PEBAX

    FDA Adverse Event
    Injury ·CONCENTRIC MEDICAL·Product code NRY·March 5, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·August 8, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·February 8, 2011