BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Reprocessed Oscillating Saw Blade, 19.5 x 90 x 0.89mm

    DI: B39050713001 · Model: 5071-300 · SURETEK MEDICAL
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Reprocessed Oscillating Saw Blade, 19.5 x 90 x 0.89mm
    Primary DI
    B39050713001
    Version / Model
    5071-300
    Company Name
    SURETEK MEDICAL
    Labeler DUNS
    785616934
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-01-05
    Public Version
    1
    Public Version Date
    2023-01-13
    Public Version Status
    New
    Public Device Record Key
    22f007ac-52c4-44f9-81a8-ca19ef726904

    Device Description

    Oscillating Saw Blade, 19.5 x 90 x 0.89mm

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

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GFA Blade, Saw, General & Plastic Surgery, Surgical

    GMDN Terms

    Code Name
    61804 Surgical saw blade, oscillating, reprocessed

    Identifiers

    Type ID
    Primary B39050713001