BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    N/A

    DI: EINO5043609 · Model: 504360 · inomed Medizintechnik GmbH
    View on AccessGUDID
    Product Codes
    2
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    N/A
    Primary DI
    EINO5043609
    Version / Model
    504360
    Company Name
    inomed Medizintechnik GmbH
    Labeler DUNS
    340782259
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-08-31
    Public Version
    3
    Public Version Date
    2022-12-14
    Public Version Status
    Update
    Public Device Record Key
    f4622eba-7040-4a37-95b9-0e796dd326ee
    Distribution End Date
    2022-12-12

    Device Description

    Sterile cover for touchscreen + C2 monitor

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

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GWF Stimulator, Electrical, Evoked Response
    ETN Stimulator, Nerve

    GMDN Terms

    Code Name
    36081 Nerve-function monitor

    Identifiers

    Type ID
    Primary EINO5043609