BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    n/a

    DI: 00874750007745 · Model: 4813 · HANS RUDOLPH, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    n/a
    Primary DI
    00874750007745
    Version / Model
    4813
    Catalog Number
    CR1775
    Company Name
    HANS RUDOLPH, INC.
    Labeler DUNS
    007131725
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-09-16
    Public Version
    5
    Public Version Date
    2023-06-30
    Public Version Status
    Update
    Public Device Record Key
    4dc2277b-7091-4b67-9f69-fa1c05fc0bd6
    Distribution End Date
    2023-06-30

    Device Description

    CUSTOM 4813:XTRA 10,&20-200LPM

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    JAX Pneumotachometer

    GMDN Terms

    Code Name
    35245 Pneumotachograph

    Identifiers

    Type ID
    Primary 00874750007745