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    FDA Registration Active 🇺🇸 United States

    SoftCheck Blood Pressure Cuff - Infant -1 Tube - ST0814FLC - 20/case

    Reg #: 2028411 · FEI: 1000125241 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    REPROCESSING PRODUCTS CORPORATION (RPC)
    Registration Number
    2028411
    FEI Number
    1000125241
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1643 W Modern Ct
    City
    TUCSON
    State
    AZ
    ZIP
    85705
    Country
    US

    Regulatory Submissions

    510(k) Number
    K940214

    Owner / Operator

    Firm Name
    REPROCESSING PRODUCTS CORPORATION (RPC)
    Operator Number
    9004570
    Address
    1643 W Modern Ct, --
    City
    Tucson
    State
    AZ
    Postal Code
    85705
    Country
    US
    Correspondent
    Brenda M Lara

    Products

    Device Name Product Code
    Blood Pressure Cuff DXQ

    Proprietary Names

    SoftCheck Blood Pressure Cuff - Infant -1 Tube - ST0814FLC - 20/case SoftCheck Blood Pressure Cuff - Large Adult Long -1 Tube - ST3544FLC - 20/case SoftCheck Blood Pressure Cuff - Child -1 Tube - ST1320FLC - 20/case SoftCheck Blood Pressure Cuff - Large Adult -1 Tube - ST3242FLC - 20/case SoftCheck Blood Pressure Cuff - Regular Adult -1 Tube - ST2635FLC - 20/case SoftCheck Blood Pressure Cuff - Thigh -1 Tube - ST4250FLC - 20/case SoftCheck Blood Pressure Cuff - Long Adult -1 Tube - ST2938FLC - 20/case SoftCheck Blood Pressure Cuff - Small Adult -1 Tube - ST1826FLC - 20/case

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device