BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    De-/Recapper 900 Flex ID, 115V

    DI: 04038917566964 · Model: 90.2060.078 · Sarstedt Aktiengesellschaft & Co.KG
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    De-/Recapper 900 Flex ID, 115V
    Primary DI
    04038917566964
    Version / Model
    90.2060.078
    Catalog Number
    90.2060.078
    Company Name
    Sarstedt Aktiengesellschaft & Co.KG
    Labeler DUNS
    388000270
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-11-30
    Public Version
    1
    Public Version Date
    2022-12-08
    Public Version Status
    New
    Public Device Record Key
    9ef878d2-20bc-4bc1-92f9-c880fe7161ca

    Device Characteristics

    Single Use
    No
    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
    Yes
    PM Exempt
    Yes
    Has Serial Number
    Yes
    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
    LXG EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE

    GMDN Terms

    Code Name
    58025 Laboratory container/microscope slide robotic transfer system IVD

    Identifiers

    Type ID
    Primary 04038917566964

    Customer Contacts

    Phone
    +1(800)257-5101
    Email
    [email protected]