BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    V. Mueller

    DI: 10885403163272 · Model: SP90-8229 · CAREFUSION 2200, INC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    V. Mueller
    Primary DI
    10885403163272
    Version / Model
    SP90-8229
    Catalog Number
    SP90-8229
    Company Name
    CAREFUSION 2200, INC
    Labeler DUNS
    832696038
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-24
    Public Version
    3
    Public Version Date
    2019-08-21
    Public Version Status
    Update
    Public Device Record Key
    6205975c-98fb-4e95-880f-f0fff9b325ff
    Distribution End Date
    2016-10-01

    Device Description

    DIAMOND-DRIVE GRASPER GATOR TOOTHED 5MM, 45CM, RATCHETED

    Device Characteristics

    Single Use
    No
    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
    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
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    GCJ Laparoscope, general & plastic surgery

    GMDN Terms

    Code Name
    35080 Rigid endoscopic tissue manipulation forceps, reusable

    Identifiers

    Type ID
    Primary 10885403163272

    Customer Contacts

    Phone
    +1(800)323-9088
    Email
    [email protected]