BEUDAMED
    32 results · 28ms · 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.

    CAMPYPAK PLUS W/PALLADIUM CATALYST DISPOS. HYDROGE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    FIBRINOGEN TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    EKG 503A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·April 23, 2014