BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    mahe medical GmbH

    DI: 04050659372191 · Model: 36.012.24SL · mahe medical gmbh
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Let the assistant research this device

    The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Brand Name
    mahe medical GmbH
    Primary DI
    04050659372191
    Version / Model
    36.012.24SL
    Company Name
    mahe medical gmbh
    Labeler DUNS
    342243334
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2019-11-05
    Public Version
    2
    Public Version Date
    2020-06-05
    Public Version Status
    Update
    Public Device Record Key
    38a3c022-9967-4f9e-83bb-a4c34ac698b1

    Device Description

    HF-knife 24CH Saline- _x000D_resectoscopy electrotrode _x000D_

    Device Characteristics

    Single Use
    Yes
    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
    No
    PM Exempt
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    Yes

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    FDC Resectoscope, working element

    GMDN Terms

    Code Name
    42551 Electrosurgical return electrode, reusable

    Identifiers

    Type ID
    Primary 04050659372191