BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Pulse® CR Aqua

    DI: 40813172023153 · Model: 194102 · INNOVATIVE HEALTHCARE CORPORATION
    View on AccessGUDID
    Product Codes
    2
    GMDN Terms
    1
    Identifiers
    3
    Pkg Device Count
    200

    Basic Information

    Brand Name
    Pulse® CR Aqua
    Primary DI
    40813172023153
    Version / Model
    194102
    Company Name
    INNOVATIVE HEALTHCARE CORPORATION
    Labeler DUNS
    802020693
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    200
    Record Status
    Published
    Publish Date
    2022-12-08
    Public Version
    2
    Public Version Date
    2023-05-03
    Public Version Status
    Update
    Public Device Record Key
    e88aa359-5681-4af0-843d-a8f69d3a9f8a

    Device Description

    Gloves, Exam, Chloroprene, Non-Sterile, Powder-Free, Textured, Aqua, S

    Device Characteristics

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    OPC Powder-Free Polychloroprene Patient Examination Glove
    LZC Patient Examination Glove, Specialty

    GMDN Terms

    Code Name
    56288 Polychloroprene examination/treatment glove, non-powdered

    Identifiers

    Type ID
    Package 30813172023156
    Primary 40813172023153
    Unit of Use 00813172023155