BEUDAMED
    FDA Registration Active 🇺🇸 United States

    40494E, Limb Clamp Electrode

    Reg #: 3016701404 · FEI: 3016701404 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    14
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Philips North America LLC
    Registration Number
    3016701404
    FEI Number
    3016701404
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1003 Corporate Lane, STE B
    City
    Export
    State
    PA
    ZIP
    15632
    Country
    US

    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
    Electrode, Electrocardiograph DRX

    Proprietary Names

    40494E, Limb Clamp Electrode QUADTRODE MRI ECG PAD,25/BOX - 989803179031 Quadtrode CV MRI ECG Electrode Pad - 989803179041 Neonatal Quadtrode MRI ECG Electrode Pad - 989803179051 BTP-1000P (Patch) Patch ePatch ECG Electrode Patch ECG Electrode Gel, ECG/EEG, Skin Prep, Tube, 3-Pack ePatch electrode MCOT Patch Patch electrode 2-CH Patch Universal Patch

    Establishment Types

    Repack or Relabel Medical Device