BEUDAMED
    10 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.

    DISPLAY MONITOR (VD-711RA-VD-712RA)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376677125·Proximity 3-Level ACP, 43 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376677132·Proximity 3-Level X-Lordotic ACP, 43 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376677156·Proximity 3-Level ACP, 43 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376677149·Proximity 3-Level X-Lordotic ACP, 43 mm

    V8 Transluminal BAV Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPROCESSED HARMONIC SCALPELS

    FDA 510(k)
    FDA Unclassified ·Unknown

    M SEREIS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 17, 2014

    BLUE RIDGE

    FDA Adverse Event
    Injury ·K2M, INC.·Product code KWQ·November 15, 2012

    BONE SCREWS, CROSS-PIN, SELF-TAPPING, DIAM.1.2X5MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code JEY·September 22, 2010