BEUDAMED
    8 results · 20ms · 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 ×

    CRYSTALLINE 'FLUORITE' CORE BUILD-UP MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    COMPACT DIGITAL CARDIAC CAMERA (CDCC)

    FDA 510(k)
    FDA Class 2 ·Radiology

    ROSA® Shoulder System

    FDA 510(k)
    FDA Class 2 ·Neurology

    ELITE PLUS LPW CUP 28/43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code JDI·August 7, 2018

    P.F.C.* 28MM HEAD +10MM

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWY·August 7, 2018

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 15, 2010

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 7

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 29, 2013

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 22, 2015