Devices & Diagnostics > Device

The PeriCoach is a perineometer designed to treat stress, mild-moderate urge and mixed urinary incontinence in women, by strengthening of the pelvic floor muscles through exercise. This device provides biofeedback via smart phone technology. The PeriCoach® device consists of a rigid probe covered in a silicone sheath that is temporarily inserted into the vagina. Sensors located under the sheath measure the strength of contraction of the user’s pelvic floor muscles. This information is then transmitted wirelessly to a smartphone application in order to provide real-time feedback to the user. It is a single patient, reusable device.


by STRATOS MEDTECH PTY LTD
Product Overview

The PeriCoach is a perineometer designed to treat stress, mild
PeriCoach® - PC0100


Device Description

A device consisting of a fluid-filled sack for intravaginal use that is attached to an external manometer. The device measures the strength of the perineal muscles by offering resistance to a patient's voluntary contractions of these muscles and is used to diagnose and to correct, through exercise, urinary incontinence or sexual dysfunction.


Environmental Conditions

  • Handling Environment Atmospheric Pressure - KiloPascal
    • 1.06
    • 0.70
  • Handling Environment Humidity - Percent (%) Relative Humidity
    • 93.00
    • 0.00
  • Handling Environment Temperature - Degrees Celsius
    • 40.00
    • 5.00
  • Storage Environment Atmospheric Pressure - KiloPascal
    • 1.06
    • 0.70
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 93.00
    • 0.00
  • Storage Environment Temperature - Degrees Celsius
    • 70.00
    • -25.00


    • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: HIR

    Device Name: Perineometer

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: GU

    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: 884.1425

    Third Party Flag: N

    Medical Specialty: OB


    Device Identifiers

    Device Id: 09338067000581

    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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