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    FDA Registration Active 🇧🇷 Brazil

    MULTIPLEX - High Resolution Esophageal/Anorectal Manometry Equipment - MULTIPLEX 36

    Reg #: 3016854619 · FEI: 3016854619 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ALACER INDUSTRIA ELETRONICA LTDA
    Registration Number
    3016854619
    FEI Number
    3016854619
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Rua Batista de Melo 113, Jardim Jabaquara
    City
    Sao Paulo
    Country
    BR

    Regulatory Submissions

    510(k) Number
    K052338

    Owner / Operator

    Firm Name
    ALACER INDUSTRIA ELETRONICA LTDA
    Operator Number
    10086657
    Address
    Rua Batista de Melo 113, Jardim Jabaquara
    City
    Sao Paulo
    State
    BR-SP
    Postal Code
    04383-080
    Country
    BR
    Correspondent
    Iracele Alkimim Sanches

    Products

    Device Name Product Code
    System, Gastrointestinal Motility (Electrical) FFX

    Proprietary Names

    MULTIPLEX - High Resolution Esophageal/Anorectal Manometry Equipment - MULTIPLEX 36 MULTIPLEX - High Resolution Esophageal/Anorectal Manometry Equipment - MULTIPLEX 24 MULTIPLEX - High Resolution Esophageal/Anorectal Manometry Equipment - MULTIPLEX 12 MULTIPLEX - High Resolution Esophageal/Anorectal Manometry Equipment - MULTIPLEX 8

    Establishment Types

    Manufacture Medical Device