BEUDAMED
    19 results · 38ms · Sources: EU EUDAMED, US FDA

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    GMI CORPORATION

    FDA registration
    GMI CORPORATION·6 products·🇺🇸 United States

    GMQ CORPORATION

    Manufacturer
    🇵🇰 Pakistan

    ZOLLNTP

    FDA Adverse Event
    Malfunction ·ZMI CORPORATION·Product code DRO·April 15, 1992

    ZOLL NTP

    FDA Adverse Event
    Death ·ZMI CORPORATION·Product code DRK·April 2, 1992

    E

    FDA Adverse Event
    Death ·ZMI CORPORATION·Product code DRO·March 26, 1992

    ZOLL PD-1200

    FDA Adverse Event
    Malfunction ·ZMI CORPORATION·Product code DRK·July 21, 1994

    ZOLL PD 1200

    FDA Adverse Event
    Malfunction ·ZMI CORPORATION·Product code DRK·July 21, 1994

    ZO11-NTP

    FDA Adverse Event
    Injury ·ZMI CORPORATION·Product code DRO·August 2, 1993

    ZOLL MEDICAL CORPORATION

    FDA Adverse Event
    Malfunction ·ZMI CORPORATION·Product code LDF·July 29, 1992

    ZOIL PACEMAKER/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZMI CORPORATION·Product code DRO·July 2, 1992

    ZOLL NTP

    FDA Adverse Event
    Death ·ZMI CORPORATION·Product code DRO·August 25, 1992

    ZOLL

    FDA Adverse Event
    Death ·ZMI CORPORATION·Product code MKJ·March 15, 1993

    1ST STEP BED

    FDA Adverse Event
    Other ·UNK·Product code INX·December 18, 1998

    LifeSync ECG System - Disposable leadwear, Ls-222, Ls-223

    FDA Recall
    Terminated ·GMP Companies/Lifesync Corporation·Product code DRG·January 10, 2007

    Triolab AS

    Importer
    🇩🇰 Denmark·11 Manufacturers

    LORCAN & FYON B.V.

    Authorized representative
    🇳🇱 Netherlands·21 Manufacturers·37 Devices

    JaviTech e.K.

    Authorized representative
    🇩🇪 Germany·111 Manufacturers·1816 Devices

    Obelis s.a.

    Authorized representative
    🇧🇪 Belgium·546 Manufacturers·18515 Devices

    SUNGO Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·1571 Manufacturers·20390 Devices