Product classification
Artificial airway atomization device
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Details Introduction
- Product Description
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[Product name] Artificial airway nebulizer
[Product model specification] LCT02-15mL-5FLCT03-22mL-5FLCT04-15mL-9FLCT05-22mL-9FLCT08-120cm
[Main structure] It consists of a breathing extension tube, with optional nebulizer cup, catheter connector, connecting straight head, and universal connector.
[Scope of application]
1. This product is used in conjunction with respiratory air supply equipment to deliver breathing gas or gas mixture to patients. Provided sterile.
2. Intended use environment: ICU ward;
3. Applicable population: patients who need respiratory treatment.
[Product performance]
1. The leakage rate should not exceed 25mL/min.
2. When the airflow resistance is tested on the pipeline at the nominal rated flow rate of 20L/min, the airflow resistance should not exceed 0.2kPa.
3. The compliance of the breathing circuit under the pressure of (6±0.3) kPa should not exceed 10mL/kPa per meter of the length of the tube.
4. Nebulization volume: Under the working condition of 6L/min airflow, the nebulization volume basically reaches the nebulization volume required for clinical nebulized inhalation drug treatment, which should be ≥0.25mL/min.
5. The product is sterile, and the residual ethylene oxide should be ≤10μg/g.
[Instructions for use]
1. Open the package, take out the product, check the product connection position, and tighten the loose connection to avoid leakage and looseness.
2. Test the product according to the guidance of the manufacturer of the respiratory air supply equipment to ensure that the product is compatible with the equipment and that the product has no leakage or blockage.
3. When nebulization treatment is required, connect the catheter connector, nebulizer cup, and breathing extension tube. Rotate and disassemble the top connecting core in the middle of the nebulizer cup, add the corresponding liquid medicine according to the doctor's instructions (the added liquid medicine should not exceed the maximum scale line of the cup body), and then install the top connecting core back; when installing the top connecting core, the bottom should not hit the small hole in the middle of the nebulizer cup, otherwise it may affect the nebulization effect. Connect one end of the catheter connector to the air source, turn on the air source, and start nebulization until the liquid medicine is nebulized. After the nebulization is completed, turn off the air source, unplug the catheter connector at one end of the air source, and tidy up the nebulizer device and dispose of it properly.
[Contraindications] Not suitable for airway nebulization inhalation treatment
【Precautions, warnings and tips】
▼This product is sterilized and packaged for single use. Do not use it if the package is damaged;
▼When the product is used in conjunction with a respiratory air supply device, ensure that the port of the respiratory air supply device matches the pipeline interface. Before use, test the product according to the instructions of the respiratory air supply device manufacturer;
▼When nebulizing, follow the doctor's instructions to use the recommended nebulizer drugs approved by clinical research;
▼Must be used or guided by professional medical staff; prevent infants and mental patients from touching it during storage or use; do not place or carry it when there is liquid medicine in the medicine cup;
▼Read the instructions carefully before use and ensure that it is used within the validity period;
▼Select the appropriate model and specifications according to the actual situation of the patient;
▼Before use, please confirm that there are no foreign objects blocking the parts;
▼This product cannot be sterilized with high temperature or high pressure;
▼Product handling method after use: harmless treatment according to the method for handling polymer medical devices;
▼When nebulization treatment is required, the recommended air pressure is 60kPa-130kPa and the gas flow rate is 6L/min.
[Storage and transportation conditions] After packaging, this product should be stored in a dry, well-ventilated, clean room with a temperature of 0-55°C, a relative humidity not exceeding 80%, and no corrosive gases. Prevent moisture, heat, direct sunlight and heavy pressure during transportation and storage, and do not freeze.
[Production date] See the product packaging
[Expiration date] Three years from the date of sterilization
[Medical device registration certificate number]
[Product technical requirements number]
[Production license number][Registrant, manufacturer and after-sales unit] Guangxi Yihe Bairui Medical Technology Co., Ltd.
[Address] Factory No. 2, No. 42, Anping Road, Guangxi-ASEAN Economic and Technological Development Zone
[Production address] Factory No. 2, No. 42, Anping Road, Guangxi-ASEAN Economic and Technological Development Zone
[Contact information] Tel: 0771-6366500
Fax:0771-6366500
Postal code: 530105
[Date of preparation of instructions]
[Explanation of label symbols]
Key words:
Hand Hygiene Disinfection | Skin and Mucous Membrane Disinfection
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