BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    VAN DELLEN ASPIRATING TUBING

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Trumpf Medical

    FDA UDI
    Baxter Medical Systems GmbH + Co. KG·00887761996021·Hospital Device

    Pads

    FDA UDI
    Baxter Medical Systems GmbH + Co. KG·00887761969452·Pad TTS Carbon 450 B

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·August 16, 2012

    SIL-V-UR CHEST CATHETER

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

    RIGHT TIME RHYTHM CLOCK

    FDA 510(k)
    FDA Unclassified ·Unknown

    MALLINKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·August 17, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·November 15, 2012

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·September 20, 2010