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

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    Pulse Oximeter (MD300C228)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPHINX JR

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

    JMS BLOOD TUBING SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    THERMOPHORE ARTHRITIS PAD

    FDA Adverse Event
    Malfunction ·BATTLE CREEK EQUIPMENT COMPANY·Product code IRT·July 22, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 6, 2014

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 18, 2013

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 4, 2014