BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LoFlo Sample Line, Adult Cannula, Box 20 - 989803183241

    Reg #: 3016701404 · FEI: 3016701404 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    9
    Establishment Types
    1
    Classifications
    2

    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

    Regulatory Submissions

    510(k) Number
    K162343

    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
    Cannula, Nasal, Oxygen CAT
    Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase CCK

    Proprietary Names

    LoFlo Sample Line, Adult Cannula, Box 20 - 989803183241 LoFlo Line, Ped Dvd Cannula, Box 100 - 989803185371 LoFlo Line, Adu Airway Adpt, Box 100 - 989803185381 LoFlo Line, Adu Airway Adpt, Box 20 - 989803183291 LoFlo Line, Ped Dvd Cannula, Box 20 - 989803183281 LoFlo Sample Line, Neo. Cannula, Box 20 - 989803183261 LoFlo Line, Adu Dvd Cannula, Box 100 - 989803185361 LoFlo Sample Line, Ped. Cannula, Box 20 - 989803183251 LoFlo Line, Adu Dvd Cannula, Box 20 - 989803183271

    Establishment Types

    Repack or Relabel Medical Device