BEUDAMED
    16 results · 28ms · Sources: EU EUDAMED, US FDA

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    JPS CORPORATION

    Manufacturer
    🇯🇵 Japan·1 Basic UDI-DI·1 Device

    JPS CORPORATION

    FDA registration
    JPS CORPORATION·1 product·🇯🇵 Japan

    NailLift

    FDA UDI
    JPS CORPORATION·04997963005783·

    NailLift

    Device
    EU MDR · Eu Md Class 1 ·JPS CORPORATION·On the market·3 countries

    NailLift

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·JPS CORPORATION·1 device

    Obelis s.a.

    Authorized representative
    🇧🇪 Belgium·546 Manufacturers·18515 Devices

    BREATHTEK UBT COLLECTION KIT

    FDA Adverse Event
    Other ·MERETEK DIAGNOSTICS, INC.·Product code MSQ·April 23, 2007

    ENDOTRACHEAL TUBE - AIRWAY MANAGEMENT

    FDA Adverse Event
    Malfunction ·UNOMEDICAL SDN BHD·Product code BTR·January 23, 2013

    BREATHTEK UBT COLLECTION KIT

    FDA Adverse Event
    Other ·MERETEK DIAGNOSTICS, INC.·Product code MSQ·January 17, 2007

    Puritan-Bennett 800 Series Ventilator Backup Power Source (BPS) Model 802, Puritan-Bennett Corporation, A subsidiary of Mallinckrodt Inc., Carlsbad, CA

    FDA Recall
    Terminated ·Covidien Limited·Product code CBK·March 21, 2008

    CL BLOOD SET Y-TYPELARGE 170-260 FILTER HAND PUMP

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE·Product code BRZ·December 30, 2010

    DPS HYPODERMIC SYRINGE LUER LOCK

    FDA Adverse Event
    Malfunction ·DPS BARE / DUOPROSS MEDITECH CORPORATION·Product code MEG·June 14, 2021

    Agfa NV

    Importer
    🇧🇪 Belgium·8 Manufacturers

    SUNGO Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·1571 Manufacturers·20390 Devices

    Emergo Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·900 Manufacturers·22100 Devices

    Wellkang Ltd

    Authorized representative
    259 Manufacturers·3500 Devices