BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    NA

    DI: 07613327064216 · Model: 0505880107 · STRYKER CORPORATION
    View on AccessGUDID
    Product Codes
    4
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    NA
    Primary DI
    07613327064216
    Version / Model
    0505880107
    Catalog Number
    0505880107
    Company Name
    STRYKER CORPORATION
    Labeler DUNS
    187502109
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-23
    Public Version
    2
    Public Version Date
    2018-03-29
    Public Version Status
    Update
    Public Device Record Key
    cc2061fe-104c-47a9-8c31-60dcc36741b6

    Device Description

    7.0 Fr., Grasping Forcep, Flexible

    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
    ["Hydrogen Peroxide", "Moist Heat or Steam Sterilization", "Ethylene Oxide"]

    Product Codes

    Code Name
    KQT EVACUATOR, GASTRO-UROLOGY
    FAS ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL
    FAJ Cystoscope and accessories, flexible/rigid
    HIH HYSTEROSCOPE (AND ACCESSORIES)

    GMDN Terms

    Code Name
    17633 Urethrotome

    Identifiers

    Type ID
    Primary 07613327064216

    Customer Contacts

    Phone
    +1(866)624-4422
    Email
    [email protected]