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    FDA UDI In Commercial Distribution 🇺🇸 United States

    Perma Pure

    DI: 00840106900381 · Model: ME Series · PERMA PURE LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    5
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Perma Pure
    Primary DI
    00840106900381
    Version / Model
    ME Series
    Catalog Number
    ME-050-03-44
    Company Name
    PERMA PURE LLC
    Labeler DUNS
    063142533
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2019-10-09
    Public Version
    2
    Public Version Date
    2022-08-05
    Public Version Status
    Update
    Public Device Record Key
    e809101a-78f5-4e6c-9b65-dcb32ba0ccce

    Device Description

    12" ME MALE SLIP & FEMALE LUER

    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
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    CBQ Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)

    GMDN Terms

    Code Name
    45566 Gas-sampling/monitoring respiratory tubing, single-use

    Identifiers

    Type ID
    Package 00840106900428
    Primary 00840106900381
    Package 00840106900411
    Package 00840106900404
    Package 00840106900398