BEUDAMED
    30 results · 26ms · Sources: EU EUDAMED, US FDA

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    HEARTSTRING III PROXIMAL SEAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STAR

    FDA UDI
    Stryker GmbH·00886385017532·TALAR M/L CUT GUIDE ASSEMBLY LEFT, MEDIUM

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014604800·BERCHTOLD B810, B710 2" STANDARD

    BARD UTRAVERSE SMALL VESSEL PTA BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NUPRO PROPHYLAXIS PASTE WITH FLUORIDE AND TRICLOSAN

    FDA 510(k)
    FDA Class 1 ·Dental

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 29, 2026

    TRIAGE PROFILER SOB PANEL 25T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·July 19, 2017

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Injury ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 13, 2019

    TRIAGE PROFILER SOB PANEL 25T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHX·August 29, 2017

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 19, 2024

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·March 4, 2021

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 3, 2018

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·January 25, 2017

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 23, 2019

    PROMOTE RF CRT-D

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·April 26, 2013

    TOTAL CARE BARIATRIC BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·April 6, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·July 21, 2008

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 5, 2018

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·January 14, 2021

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 31, 2019