BEUDAMED
    FDA Registration Active 🇺🇸 United States

    M1870B Neonatal Single-Patient Cuff Size #3

    Reg #: 3016618143 · FEI: 3016618143 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Philips North America LLC
    Registration Number
    3016618143
    FEI Number
    3016618143
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    222 Jacobs Street
    City
    Cambridge
    State
    MA
    ZIP
    02141
    Country
    US

    Regulatory Submissions

    510(k) Number
    K905101

    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
    Blood Pressure Cuff DXQ

    Proprietary Names

    M1870B Neonatal Single-Patient Cuff Size #3 M1866B Neonatal Single-Patient Cuff Size #1 M1872S Neonatal Soft Single-Patient Cuff Size#4 M1872B Neonatal Single-Patient Cuff Size #4 M1870S Neonatal Soft Single-Patient Cuff Size#3 M1873S Infant Soft Single-Patient Cuff Size #5 M1868B Neonatal Single-Patient Cuff Size #2 M1866S Neonatal Soft Single-Patient Cuff Size#1 989803167541 Neonatal Single-Patient NIBP Cuffs 989803167551 Neonatal Soft Single-Patient NIBP Cuffs M1873B Infant Single-Patient Cuff Size #5 M1868S Neonatal Soft Single-Patient Cuff Size#2

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility