BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    ADVANCED PATIENT MONITOR

    DI: B510PM2000A1 · Model: PM-2000A · ADVANCED INSTRUMENTATIONS, INC.
    View on AccessGUDID
    Product Codes
    8
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    ADVANCED PATIENT MONITOR
    Primary DI
    B510PM2000A1
    Version / Model
    PM-2000A
    Company Name
    ADVANCED INSTRUMENTATIONS, INC.
    Labeler DUNS
    608736880
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-04-16
    Public Version
    3
    Public Version Date
    2021-11-10
    Public Version Status
    Update
    Public Device Record Key
    d6c3ea34-f3e0-4fd0-b15d-96033f335811
    Distribution End Date
    2028-04-15

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    No
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    DQA Oximeter
    DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
    DSA Cable, Transducer And Electrode, Patient, (Including Connector)
    DSI Detector And Alarm, Arrhythmia
    DSK Computer, Blood-Pressure
    DXN System, Measurement, Blood-Pressure, Non-Invasive
    FLL Thermometer, Electronic, Clinical
    MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    GMDN Terms

    Code Name
    36872 Multiple vital physiological parameter monitoring system, clinical

    Identifiers

    Type ID
    Primary B510PM2000A1

    Premarket Submissions

    Submission Number Supplement Number
    K123048 000