BEUDAMED
    FDA Registration Active 🇺🇸 United States

    PM-2000M Patient Monitor

    Reg #: 1066270 · FEI: 3000957797 · Expires 2025
    View on FDA
    Products
    14
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    14

    Registration Details

    Registration Name
    ADVANCED INSTRUMENTATIONS, INC.
    Registration Number
    1066270
    FEI Number
    3000957797
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6800 NW 77TH COURT
    City
    Miami
    State
    FL
    ZIP
    33166
    Country
    US

    Regulatory Submissions

    510(k) Number
    K132077

    Owner / Operator

    Firm Name
    ADVANCED INSTRUMENTATIONS, INC.
    Operator Number
    9044980
    Address
    6800 NW 77TH COURT, --
    City
    Miami
    State
    FL
    Postal Code
    33166
    Country
    US
    Correspondent
    Rafael Celli

    Products

    Device Name Product Code
    System, Measurement, Blood-Pressure, Non-Invasive DXN
    Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) MHX
    Monitor, St Segment With Alarm MLD
    Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) DRT
    Computer, Blood-Pressure DSK
    Analyzer, Gas, Oxygen, Gaseous-Phase CCL
    Detector And Alarm, Arrhythmia DSI
    Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration) CBQ
    Cable, Transducer And Electrode, Patient, (Including Connector) DSA
    Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.) CBS
    Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase CCK
    Oximeter DQA
    Continuous Measurement Thermometer FLL
    Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.) CBR

    Proprietary Names

    PM-2000M Patient Monitor

    Establishment Types

    Manufacture Medical Device