BEUDAMED
    9 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 ×

    CHEK-STIX U.T.I. SELF-TEST

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AZO

    FDA Adverse Event
    Other ·SIEMENS DIAGNOSTICS, INC.·Product code CEN·July 12, 2012

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295234418·P.F.C. SIGMA POSTERIOR AUGMENT COMBO CEMENTED S...

    MODEL 6/60 CRT VIDEO-SONAR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ACELL POWDER WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    PROULTRA ENDO TIPS

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code ELC·June 8, 2006

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·June 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 30, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 12, 2011