BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    CEDIA PROCAINAMIDE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149878·K-WIRE - DOUBLE TROCAR FULLY THREADED 2.0mm DIA...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471155978·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 230mm

    DRILL SLEEVE F. SOLID STEPDRILL

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·February 23, 2012

    IBS Implant System II

    FDA 510(k)
    FDA Class 2 ·Dental

    PHASE 3, MODEL DT-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLINITEK 500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CHL·January 22, 2013

    ETS FLEX ARTICNG

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 17, 2011

    ASR TAP SLV ADAP 12/14 -1

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 28, 2014