BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    SURGICAL STERILE DRAPE

    DI: 08056646501663 · Model: 12.A1028.00 · OMNIA SRL
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    30

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    Basic Information

    Brand Name
    SURGICAL STERILE DRAPE
    Primary DI
    08056646501663
    Version / Model
    12.A1028.00
    Company Name
    OMNIA SRL
    Labeler DUNS
    447696675
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    30
    Record Status
    Published
    Publish Date
    2016-09-11
    Public Version
    6
    Public Version Date
    2021-12-22
    Public Version Status
    Update
    Public Device Record Key
    9e9cd3e9-c5b7-499e-84cd-406acffce2aa

    Device Description

    LIQUID PROOF DRAPE CM 145X160 - BLUE

    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
    KKX Drape, Surgical

    GMDN Terms

    Code Name
    47783 Patient surgical drape, single-use

    Identifiers

    Type ID
    Primary 08056646501663
    Unit of Use 08056646501656

    Customer Contacts

    Phone
    +390524527453
    Email
    [email protected]