BEUDAMED
    FDA Registration Active 🇺🇸 United States

    M5072A Infant/Child SMART Pads Cartridge

    Reg #: 3030677 · FEI: 1000524572 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Philips North America LLC
    Registration Number
    3030677
    FEI Number
    1000524572
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    22100 Bothell Everett Hwy
    City
    Bothell
    State
    WA
    ZIP
    98021
    Country
    US

    Regulatory Submissions

    PMA Number
    P160029

    Owner / Operator

    Firm Name
    Philips Medical Systems International BV
    Operator Number
    1217116
    Address
    Veenpluis 6
    City
    Best
    State
    NL-NOTA
    Postal Code
    5684PC
    Country
    NL

    Products

    Device Name Product Code
    Automated External Defibrillators (Non-Wearable) MKJ
    Over-The-Counter Automated External Defibrillator NSA

    Proprietary Names

    M5072A Infant/Child SMART Pads Cartridge M5068A HeartStart Home Defibrillator M5071A Adult SMART Pads Cartridge M5066A HeartStart Onsite Defibrillator M5070A Primary Battery

    Establishment Types

    Manufacture Medical Device