BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Welch Allyn, Inc.

    DI: 00732094009125 · Model: 901055 · WELCH ALLYN, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Welch Allyn, Inc.
    Primary DI
    00732094009125
    Version / Model
    901055
    Catalog Number
    34XF-EX
    Company Name
    WELCH ALLYN, INC.
    Labeler DUNS
    198227881
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2021-05-07
    Public Version
    2
    Public Version Date
    2022-06-27
    Public Version Status
    Update
    Public Device Record Key
    97c6bf27-a170-4ea1-a134-74e659331d89

    Device Description

    PROBP 3400 STANDARD W SUREBP EXCHANGE

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    DQA Oximeter

    GMDN Terms

    Code Name
    45617 Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

    Identifiers

    Type ID
    Primary 00732094009125

    Customer Contacts

    Phone
    +1(315)685-2834
    Email
    [email protected]