BEUDAMED
    8 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    TEST KIT, IIF-AMA

    FDA 510(k)
    FDA Class 2 ·Immunology

    equilibrium®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790295020·equilibrium® 2 Band bracket with hook, - 11° T...

    Confirm Rx Insertable Cardiac Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BODYVIZ, MODEL 100

    FDA 510(k)
    FDA Class 2 ·Radiology

    2.0MM DRILL BIT/QC/125MM

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HWE·May 5, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 15, 2012

    TALENT ABDOMINAL STENT GRAFT SYSTEM - HYDRO

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·August 6, 2010

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

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