BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    LEECO PROGESTERONE-QUANT DIAGNOSTIC TEST KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376249506·Occipital Plate, 56mm

    Luxisse+

    FDA 510(k)
    FDA Class 2 ·Dental

    MODEL 2500A PALMSAT PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASR XL ANATOMIC HEAD SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·June 4, 2014

    STERLING¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·November 29, 2012

    SM104 M-SERIES W/5TH WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIV.·Product code FPO·September 27, 2010

    INVICTUS

    FDA Adverse Event
    Injury ·ALPHATEC SPINE, INC.·Product code NKG·June 17, 2021

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012