BEUDAMED
    24 results · 24ms · 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 ×

    MODIFICATION TO CODMAN HAKIM SHUNT SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Prodigy Control Solution High

    FDA UDI
    Prodigy Diabetes Care, LLC·00384840533509·Prodigy Control Solution High 4mL

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809841985·FOR MEN 30-40 MM HG KNEE HIGH CLOSED TOE LARGE ...

    HEALTH-PLUS, SANITEX, RELIANCE MULTIPLY POWDER FREE POLYMER AND NITRILE COATED (BLUE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO DEPUY C-STEM SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® FA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWS·April 11, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 13, 2011

    INVACARE LIFTS AND SLINGS

    FDA Adverse Event
    Injury ·INVACARE CORPORATION - MANUFACTURING FACILITY·Product code FSA·May 28, 2008

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code MDB·August 16, 2019