BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    NA

    DI: 04042409042256 · Model: IU 8002-00 · aap Implantate AG
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    NA
    Primary DI
    04042409042256
    Version / Model
    IU 8002-00
    Company Name
    aap Implantate AG
    Labeler DUNS
    328420633
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-02-28
    Public Version
    2
    Public Version Date
    2018-06-11
    Public Version Status
    Update
    Public Device Record Key
    d52125cd-75a2-40eb-930e-d48ffacc952f

    Device Description

    Screw forceps, long

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    HTD FORCEPS

    GMDN Terms

    Code Name
    42894 Implant handling forceps, scissors-like

    Identifiers

    Type ID
    Primary 04042409042256