BEUDAMED
    FDA Registration Active 🇨🇷 Costa Rica

    Sub-Assembly, Cannula, RCSP, Silicone, w/ Manual Inflating Elongated Smooth Cuff, Guidewire Style Stylet, 15 FR

    Reg #: 3005173255 · FEI: 3005173255 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Viant Costa Rica, S.A.
    Registration Number
    3005173255
    FEI Number
    3005173255
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Parque Zona Franca Metropolitana, Edificio 2C
    City
    BARREAL DE HEREDIA
    Country
    CR

    Regulatory Submissions

    510(k) Number
    K953945

    Owner / Operator

    Firm Name
    Viant Medical, LLC
    Operator Number
    9043339
    Address
    2 Hampshire Street, Suite 202
    City
    Foxborough
    State
    MA
    Postal Code
    02035
    Country
    US
    Correspondent
    David - Rose

    Products

    Device Name Product Code
    Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass DWF

    Proprietary Names

    Sub-Assembly, Cannula, RCSP, Silicone, w/ Manual Inflating Elongated Smooth Cuff, Guidewire Style Stylet, 15 FR Sub-Assembly, Cannula, RCSP, Silicone, with Manual Inflating MR20 Ridged Cuff, Guidewire Style Stylet, 15 FR Sub-Assembly, Cannula, RCSP, Silicone, w/ Manual Inflating MR20 Ridged Cuff, Ext Press Monitoring & Inflation Lines, 13 Sub-Assembly, Cannula, RCSP, Silicone, w/ Manual Inflating Ridged Cuff, Guidewire Stylet, Tru-touch Handle, 15FR Sub-Assembly, Cannula, RCSP, Silicone, w/ Manual Inflating Ridged Cuff, Solid Stylet, Tru-touch Handle, 15FR Sub-Assembly, Cannula, RCSP, Gundry, Silicone, w/ Manual Inflating MR20 Ridged Cuff, Guidewire Stylet,13 FR Sub-Assembly, Cannula, RCSP, Silicone, with Manual Inflating Elongated Smooth Cuff, Solid Stylet, 15 FR

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)