BEUDAMED
    FDA Registration Active 🇺🇸 United States

    REVIVER AED

    Reg #: 3003521780 · FEI: 3003521780 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    DEFIBTECH, LLC
    Registration Number
    3003521780
    FEI Number
    3003521780
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    741 BOSTON POST ROAD,SUITE 201
    City
    GUILFORD
    State
    CT
    ZIP
    06437
    Country
    US

    Regulatory Submissions

    510(k) Number
    K033896

    Owner / Operator

    Firm Name
    DEFIBTECH, LLC
    Operator Number
    9048526
    Address
    741 BOSTON POST ROAD, SUITE 201
    City
    Guilford
    State
    CT
    Postal Code
    06437
    Country
    US
    Correspondent
    Robert Jamieson

    Products

    Device Name Product Code
    Automated External Defibrillators (Non-Wearable) MKJ
    Electrode, Electrocardiograph, Multi-Function MLN

    Proprietary Names

    REVIVER AED ADAPTER MONITOR PADS DEFIBTECH AED WITH ATTENUATED DEFIB LIFELINE ELECTRODE ADAPTER

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility