BEUDAMED
    14 results · 24ms · Sources: EU EUDAMED, US FDA

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    AUTOMATED GYLCOHEMOGLOBIN ANALYZER HLC-723G8

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

    G8

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC, INC.·Product code PDJ·August 27, 2025

    NC Screw-retained Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600303428·

    ArgenIS

    FDA UDI
    ARGEN CORPORATION, THE·D81813580·TiBase ZS RP 1.5G E

    NON-STERILE, POWDER-FREE, BLUE COLOR NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NEV'S INK AUTOCLAVE TAPES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POWER CORE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS, INSTRUMENTS DIV·Product code HWE·May 20, 2013

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 1, 2014

    CAPSURE VDD-2

    FDA Adverse Event
    Injury ·MPRI·Product code DXY·June 16, 2011

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 22, 2022