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    【Case Study】Nasal Irrigator Registration in China

    from CIRS by

    1. Introduction

    Product Name: nasal irrigator, nasal wash

    Product Composition: consists of a main unit, a water tank, a nasal wash (adult and child type), and a power adapter.

    Working Principle:

    After the nasal irrigator is energized, the motor converts the electrical energy into mechanical pressure. The pressure is used to deliver warm water/physiological saline into the nostrils, through the nasal vestibule, sinus, and nasal passages around the nasopharynx, and from the other side of the nostrils. Through the above path, the sterilizing action of the physiological saline itself and the impact force of the water flow are used to discharge the accumulated dirt and harmful substances in the nasal cavity, thereby achieving the purpose of cleaning and daily care of the nasal cavity.

    Typical Structure:

    Nasal Irrigator

    Adult type Child type

    No.

    Name

    Description

    1

    Head

    The outlet of the water flow controls the water volume stably and sprays evenly

    2

    Nozzle release button

    Use and pause control buttons

    3

    Host

    Control the operation of the nasal irrigator

    4

    Rotary switch

    Adjustment circuit closure

    5

    Water tank

    Water storage

    6

    Power adapter

    Connected to the power supply

    Scope of application: For nasal irrigation and daily nasal hygiene

    Applicable people: Suitable for adults and children with nasal cleansing needs

    2. Classification

    Classification Code: 14-07-01 Class II Flushing device

    Product Description: Usually composed of a host, a heating module, and a power module

    Expected Usage: For rinsing the natural cavity (excluding vaginal), rinsing the tissue during and after surgery, and warming the rinsing fluid

    3. Registration Unit

    1. Different principle

    Passive polymer material nasal irrigators and active electric irrigators cannot be registered together.

    2. Sterile and non-sterile

    The polymer material type irrigator is a class II device provided by sterilizing, and a class I device provided by non-sterile; the electric nasal lavage device is class II.

    3. Whether it contains drugs

    Separate registration with medicinal ingredients and without drugs.

    4. Technical Requirements

    1. Appearance

    The appearance of the nasal irrigator should be neat, smooth and uniform in color; no defects such as sharp edges, burrs, cracks, etc.; the characters and signs on the panel should be clearly visible; the installation and connection parts should be tight, the movable parts should be used, the rotation is flexible and reliable; the water tank is leak-free. .

    2. Tank capacity

    The water tank capacity is 700ml.

    3. Flushing pressure

    The water pressure at the outlet of the nasal wash should be between 0.1 MPa and 0.3 MPa.

    4. Flushing flow rate

    The water flow rate at the outlet of the nasal wash should be no more than 10 ml/s.

    5. Flush height

    The outlet height of the adult nasal wash outlet is 4.0 cm ± 1.0 cm; the height of the child's nasal wash outlet is 2.0 cm ± 1.0 cm.

    6. Irrigator piping system effluent chemical properties

    6.1 pH

    The difference between the pH of the eluate and the blank control solution should be ≤1.0;

    6.2 Heavy metal content

    The heavy metal content of the eluate should be ≤1.0 μg/mL.

    7. Electrical safety requirements

    Should meet the requirements of GB9706.1-2007.

    8. Electromagnetic compatibility requirements

    Should meet the requirements specified in YY 0505-2012.

    9. Environmental test requirements

    It should meet the requirements of the climatic environment test group II and the mechanical environment group II in GB/T 14710-2009.

    Table 1 Relevant Product Standards

    Standard Number

    Standard Name

    GB/T 191-2008

    Packaging storage and transportation icon

    YY/T 0316-2016

    Medical device risk management for medical devices

    YY/T 0466.1-2009

    Medical devices - Symbols for labeling, marking and providing information on medical devices - Part 1: General requirements

    GB/T 14710-2009

    Medical electrical environment requirements and test methods

    GB 9706.1-2007

    Medical electrical equipment - Part 1: General requirements for safety

    YY 0505-2012

    Medical electrical equipment - Part 1-2: Safety commons Parallel standard: Electromagnetic compatibility Requirements and testing

    GB/T 14233.1-2008

    Medical infusion, blood transfusion, injectables - Test methods - Part 1

    YY(/T): Industry standard (Recommendation)

    GB(/T): National standard (Recommendation)

    5. Clinical Trials

    Clinical Trials: required

    6. Registration Cost and Duration

    1) Product Testing

    Test items

    Testing duration

    Testing fee(USD)

    Safety Performance

    60 working days

    3,000

    EMC (Internal and external circuits )

    90 working days

    4,500*2

    Biocompatibility

    60 working days

    3,500

    2) Technology Approval

    60 working days

    Another 60 working days if the 1-year supplement is required

    3) Administrative Approval

    20 working days

    If you would like to get the detailed registration proposal, please contact us via md@cirs-group.com.

      

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    Contact Us
    +86 571 8720 6559 (GMT+8 8:30~17:00)
    Contact Us
    +86 571 8720 6559 (GMT+8 8:30~17:00)
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