BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Protekt Pulse

    DI: 05060488570308 · Model: 20120 · PROACTIVE MEDICAL PRODUCTS, LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Protekt Pulse
    Primary DI
    05060488570308
    Version / Model
    20120
    Catalog Number
    20120
    Company Name
    PROACTIVE MEDICAL PRODUCTS, LLC
    Labeler DUNS
    078582655
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-08-12
    Public Version
    3
    Public Version Date
    2021-11-10
    Public Version Status
    Update
    Public Device Record Key
    0607a851-10df-44d9-b80a-c5df8e66c73d

    Device Description

    DELUXE RECHARGEABLE HANDHELD PULSE OXIMETER

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    DQA Oximeter

    GMDN Terms

    Code Name
    45607 Pulse oximeter

    Identifiers

    Type ID
    Primary 05060488570308

    Customer Contacts

    Phone
    +1 855 237 7622
    Email
    [email protected]

    Device Sizes

    Type Value Unit Text
    Height 1.5 Inch
    Length 3.5 Inch
    Width 6 Inch