BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    ADULT ULTRA FLEX®

    DI: 00612649215686 · Model: F92102 · King Systems Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    ADULT ULTRA FLEX®
    Primary DI
    00612649215686
    Version / Model
    F92102
    Catalog Number
    F92102
    Company Name
    King Systems Corporation
    Labeler DUNS
    009299017
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2021-04-12
    Public Version
    2
    Public Version Date
    2022-10-24
    Public Version Status
    Update
    Public Device Record Key
    02a2b1e5-1251-4ad4-9bee-236b5fff6df5

    Device Description

    ADULT ULTRA FLEX CIRCUIT PACK KIT

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    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
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    CAI Circuit, breathing (w connector, adaptor, y piece)

    GMDN Terms

    Code Name
    37704 Anaesthesia breathing circuit, single-use

    Identifiers

    Type ID
    Package 00612649215679
    Primary 00612649215686

    Customer Contacts

    Phone
    +14107686464
    Email
    [email protected]

    Device Sizes

    Type Value Unit Text
    Device Size Text, specify Adult