BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    IntelliVue Patient Monitors MX100, MX400, MX430, MX450, MX500, MX550, IntelliVue Patient Monitors MX700, MX800, IntelliVue Patient Monitors MP5, MP5SC, Multi-Measurement Module X3

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PMT CORP.

    FDA registration
    PMT CORP.·23 products·🇺🇸 United States

    S8 ADVANCE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEXGEN PERIPHERAL GUIDE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    XIA BLOCKER

    FDA Adverse Event
    Injury ·STRYKER SPINE-SWITZERLAND·Product code KWP·June 21, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·July 28, 2011

    SPECTRANETICS GLIDELIGHT LASER SHEATH

    FDA Adverse Event
    Death ·SPECTRANETICS CORPORATION·Product code MFA·October 17, 2014

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·November 10, 2021

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 15, 2026