BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    EGERTON TURNING & TILTING NET SUSPEN BED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172971109·

    EASY COMFORT DELUXE MANUAL BREAST PUMP, MODEL 1187

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    IPL Cooling Hair Removal Device

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

    PLUM A+ DRIVER NEW

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 17, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 14, 2012

    LIBERTE' CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·September 13, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018