BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    PUL,MONARY ARTERY VENT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    Zimmer, Inc.·00889024102521·

    NA

    FDA UDI
    Zimmer, Inc.·00889024102538·

    PRESSURIZING/SCAVENGING ACRYLIC CEMENT

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    RELIANCE TREATMENT CABINET

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 4, 2012

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 19, 2013

    NA

    FDA UDI
    Zimmer, Inc.·00889024074811·

    NA

    FDA UDI
    Zimmer, Inc.·00889024074804·

    NA

    FDA UDI
    Zimmer, Inc.·00889024074798·

    UNIVERSAL DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·June 3, 2014

    NAVILYST MEDICAL

    FDA Adverse Event
    Malfunction ·NAVILYST MEDICAL·Product code LJS·October 25, 2012

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DRY·September 13, 2010