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

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    Surefire Infusion System 021

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013402422·MARKS NEEDLE, #18

    MYLAB 15 / MYLAB 20, MODEL 2700

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPECTRA LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VALEO / VALEO II

    FDA Adverse Event
    Malfunction ·SINTX TECHNOLOGIES (FORMERLY AMEDICA CORP)·Product code MAX·March 25, 2020

    1020279-2014-00617

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 6, 2014

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 3, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 29, 2011