BEUDAMED
    FDA Registration Active 🇺🇸 United States

    VENTANA PD-L1 (SP142) Assay W

    Reg #: 2028492 · FEI: 1000125183 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    10
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    VENTANA MEDICAL SYSTEMS, INC.
    Registration Number
    2028492
    FEI Number
    1000125183
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1910 EAST INNOVATION PARK DR.
    City
    Tucson
    State
    AZ
    ZIP
    85755
    Country
    US

    Owner / Operator

    Firm Name
    Roche Diagnostics Operations Inc.
    Operator Number
    9039767
    Address
    9115 Hague Road
    City
    Indianapolis
    State
    IN
    Postal Code
    46250
    Country
    US

    Products

    Device Name Product Code
    Immunohistochemistry Reagents And Kits NJT

    Proprietary Names

    VENTANA PD-L1 (SP142) Assay W NEXES VEN IVIEW DAB DET KT JPN-US Export CINtec PLUS Cytology Kit (US-Export) VENTANA PD-L1 (SP263) CE IVD US Export CINtec PLUS Cytology Kit (CE IVD) VEN anti-HER2/neu [4B5] RM PAB-US EXPORT VENTANA ROS1 (SP384) Assay US Export VENTANA CLDN18 (43-14A) RxDx Assay VENTANA EBER Probe VENTANA CLDN18 (43-14A) RxDx Assay W

    Establishment Types

    Manufacture Device in the United States for Export Only