BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    DRESSING CHANG & WOUND MANAGEMENT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE

    RBM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    GORE(R) EMBOLIC FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TOTAL ASR ACET IMP SIZE 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·January 17, 2013

    ZEPHYR XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2015