BEUDAMED
    2,352 results · 39ms · Sources: EU EUDAMED, US FDA

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    Philips France Commercial

    Manufacturer
    🇫🇷 France·1 Basic UDI-DI·1 Device

    Philips France

    FDA registration
    Philips France·5 products·🇫🇷 France

    PHILIPS FRANCE

    FDA registration
    PHILIPS FRANCE·2 products·🇫🇷 France

    Cardiologs Platform

    FDA UDI
    PHILIPS FRANCE·00884838131958·

    Cardiologs Platform

    FDA UDI
    PHILIPS FRANCE·G637CEA0·

    Cardiologs Platform

    Device
    EU MDR · Eu Md Class 2a ·Philips France Commercial·On the market·12 countries

    PHILIPS FR/FR2/FR2+ Adult Electrode Pads

    FDA UDI
    PHILIPS ELECTRONICS NORTH AMERICA CORPORATION·00884838029569·5-pack HS FR/FR2 Defib Pads (DP2/DP6)

    PHILIPS FR/FR2/FR2+ Adult Electrode Pads

    FDA UDI
    PHILIPS ELECTRONICS NORTH AMERICA CORPORATION·00884838023727·HeartStart DP Pads, 5 sets

    CARDIOLOGS PLATFORM V2.4.7

    FDA Adverse Event
    Injury ·PHILIPS FRANCE·Product code DPS·October 3, 2025

    CARDIOLOGS PLATFORM - V2.4.10A

    FDA Adverse Event
    Injury ·PHILIPS FRANCE·Product code DPS·July 1, 2025

    CARDIOLOGS PLATFORM - V2.4.10A

    FDA Adverse Event
    Injury ·PHILIPS FRANCE COMMERICAL·Product code DPS·August 8, 2025

    CARDIOLOGS PLATFORM - V 2.4.8A

    FDA Adverse Event
    Death ·PHILIPS FRANCE COMMERICAL·Product code DPS·October 7, 2025

    CARDIOLOGS PLATFORM V2.3.13

    FDA Adverse Event
    Death ·PHILIPS FRANCE COMMERICAL·Product code DPS·October 21, 2025

    CARDIOLOGS PLATFORM V2.3.13

    FDA Adverse Event
    Death ·PHILIPS FRANCE COMMERICAL·Product code DPS·October 21, 2025

    CARDIOLOGS HOLTER PLATFORM

    FDA Adverse Event
    Death ·PHILIPS FRANCE COMMERICAL·Product code DPS·April 17, 2023

    CARDIOLOGS PLATFORM, VERISON 2.4.3

    FDA Adverse Event
    Injury ·PHILIPS FRANCE COMMERICAL·Product code DPS·May 5, 2025

    TEMPUS PRO, BT HEADSET DOCK

    FDA Adverse Event
    Malfunction ·REMOTE DIAGNOSTIC TECHNOLOGIES LTD.·Product code MHX·September 24, 2025

    Cardiologs Platform

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Philips France Commercial·1 device

    ALLURA XPER FD10

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·April 18, 2017

    TEMPUS PRO

    FDA Adverse Event
    Malfunction ·REMOTE DIAGNOSTIC TECHNOLOGIES LTD.·Product code MHX·January 30, 2024