BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    ELI 280 ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ArgenZ HT+ 98x22 A1-L

    FDA UDI
    ARGEN CORPORATION, THE·D818122073·Dental porcelain/ceramic restoration kit

    MONOSYN VIOLET 1 (4) 90CM HS37S (M)

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·July 29, 2022

    HEARTLINE RECEIVING STATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MED-RX TRANSFER SET, MODELS 10-1227TS, 10-1300TS, 10-1305TS AND 10-1306TS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD·Product code HQL·May 16, 2013

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 26, 2014

    DRILL GUIDE FOR DIAM 3.5 SCREW

    FDA Adverse Event
    Malfunction ·INTEGRA, SAINT PRIEST·Product code HTW·May 24, 2011

    WEBSTER CS CATHETER WITH EZ-STEER TECHNOLOGY AND AUTO ID

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·June 4, 2013

    QUADRA C FEMORAL STEM SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·October 22, 2012

    MONOSYN VIOLET 5/0 (1) 70CM HR17 (M).RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·October 19, 2023