KoKo Sx 1000 spirometer and software package, fully compatible with Iris server to allow support for networked data access, patient questionnaires, workflow, and HL7 connectivity.


Product Overview

KoKo Sx 1000 spirometer and software package, fully compatible with Iris server to allow support for networked data access, patient questionnaires, workflow, and HL7 connectivity.
nSpire Health - KoKo Sx 1000 Diagnostic Spirometer


Device Description

An electrically-powered device designed exclusively for professional use to measure several or all respiratory gas volume and flow parameters for evaluation of basic pulmonary function [e.g., vital capacity (VC), peak expiratory flow (PEF), forced expiratory volume (FEV), and forced expiratory flow (FEF)]; it may also perform pulse oximetry. It is typically a hand-held instrument with a mouthpiece which communicates with a computerized unit (e.g., analysis system, graph recorder, tablet). It is used to help diagnosis and monitoring of chronic pulmonary disorders such as asthma, emphysema, or bronchitis, and potentially heart disorders.


Environmental Conditions

  • Handling Environment Atmospheric Pressure - Millimeter of Mercury
    • 780.00
    • 550.00
  • Handling Environment Humidity - Percent (%) Relative Humidity
    • 95.00
    • 0.00
  • Handling Environment Temperature - Degrees Celsius
    • 50.00
    • -20.00
  • Storage Environment Atmospheric Pressure - Millimeter of Mercury
    • 780.00
    • 550.00
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 95.00
    • 0.00
  • Storage Environment Temperature - Degrees Celsius
    • 50.00
    • -20.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: BZG

    Device Name: Spirometer, Diagnostic

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: AN

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 868.1840

    Third Party Flag: Y

    Medical Specialty: AN


    Device Identifiers

    Device Id: 00852417003347

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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