BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    THEKEN ATOLL CERVICO-THORACIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRIO LX SMALL CONNECTOR

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·March 23, 2011

    RESPONDER 3000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    NEUROPLUS, MODEL A10040, A10041, A10042, A10043

    FDA 510(k)
    FDA Class 2 ·Neurology

    MULTIPOLAR BIPOLAR SHELL 50 MM O.D.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code KWY·June 4, 2024

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code OTN·April 12, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·April 27, 2011

    PROXIMATE RH REG SKIN STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·July 1, 2008