BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Maximo® II DR

    DI: 00613994446602 · Model: D284DRG · MEDTRONIC, INC.
    View on AccessGUDID
    Product Codes
    2
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Maximo® II DR
    Primary DI
    00613994446602
    Version / Model
    D284DRG
    Company Name
    MEDTRONIC, INC.
    Labeler DUNS
    006261481
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2014-09-23
    Public Version
    4
    Public Version Date
    2023-07-31
    Public Version Status
    Update
    Public Device Record Key
    d2b8874c-6bcf-4838-8942-587cb4dc769b
    Distribution End Date
    2023-07-05

    Device Description

    ICD-DR D284DRG Maximo II DF-1 US

    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
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    NIK Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
    LWS Implantable cardioverter defibrillator (non-CRT)

    GMDN Terms

    Code Name
    37265 Dual-chamber implantable defibrillator

    Identifiers

    Type ID
    Primary 00613994446602

    Customer Contacts

    Phone
    +1(800)633-8766
    Email
    [email protected]

    Storage Conditions

    Type
    Storage Environment Temperature
    Temperature Range
    0 – 131 Degrees Fahrenheit