BEUDAMED
    11 results · 23ms · 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 ×

    CHOLESTEROL ENZYMATIC ENDPOINT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AirLife™

    FDA UDI
    AIRLIFE·10889483587249·AirLife™ Isothermal™ Breathing Circuit Accessor...

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111109·INSTRUMENT CASE DOUBLE ALUMINUM

    Ceribell Status Epilepticus Monitor

    FDA 510(k)
    FDA Class 2 ·Neurology

    MODIFICATION TO ATB ALL-TERRAIN BALLOON PTA DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code CGA·July 27, 2016

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·January 22, 2013

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GHH·December 14, 2010

    ISOFLEX OPTIM LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·July 9, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·October 19, 2016

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·July 26, 2016