BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    ASAHI HOLLOW FIBER KIDNEYS, AM-SERIES

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

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776412944·Egress Cannula Blunt Obturator 2.3mm

    CORONARY ARTERY PERFUSION CANNULA WITH SELF-INFLATING BALLOON

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NON-CONTACT INFRARED THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RADIAL JAW 4 JUMBO BIOPSY FORCEPS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNW·March 25, 2008

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 12, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 13, 2012

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·September 2, 2010

    WALLSTENT ENTERAL ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC IRELAND LTD.·Product code MQR·April 3, 2008

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015