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

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    RS85 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 15, 2022

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 15, 2022

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·September 7, 2022

    CPS AIM SL SLITTABLE INNER CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRANSTEK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 17, 2014

    HOLLOW-REAMER-COMPL ANTICLOCKWISE CUTTIN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·June 21, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 28, 2011

    BAXJECT II HI-FLOW

    FDA Adverse Event
    Malfunction ·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026