BEUDAMED
    9 results · 27ms · 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.

    DADE LOW IONIC STRENGTH SOLUITION (LISS)

    FDA 510(k)
    FDA Class 2 ·Hematology

    MEGAPULSE LASER SYSTEM AND FIBERS

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

    IMPEDANCE TESTER (MODEL 4390)

    FDA 510(k)

    TI MATRIXNEURO SCREW SELF-DRILLING 4MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·May 5, 2014

    ADAPTA VDD

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NVZ·October 15, 2012

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE(SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·August 4, 2010

    OT VERIO TEST STRIP

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code CGA·March 25, 2022

    OT VERIO TEST STRIP

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code CGA·March 30, 2022

    Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065; CD3215-36Q/100004059, 100004060, 100004061, 100023304, 100030590, 100033678, 100042492, 100046803, 100046906

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