Video-enabled double-lumen endotracheal intubation ISO13485
certified
Product Introduction
The double-lumen endobronchial tube is an airway management device
designed specifically for thoracic surgery, achieving single-lung
ventilation through a unique sub-lumen structure. The main body of
the product is made of medical-grade PVC material and contains two
independent channels, the bronchial cavity and the tracheal cavity,
with blue and transparent connectors for easy identification. The
front end of the catheter is anatomically curved and equipped with
a high-definition video channel (1.2mm diameter), which can be
connected to an endoscope for real-time visual positioning. The
airbag adopts a low-pressure and high-volume design, and the
injection pressure does not exceed 25cmH₂O, reducing the risk of
airway mucosal damage. The product complies with the ISO13485
quality management system and has obtained CE and FDA
certification. It is suitable for thoracoscopic surgery, lobectomy
and other precision operations that require lung isolation.
Parameter table/selection table
Size(FR) | CODE |
Left | Right |
28 | MC-09KL28 | MC-09KR28 |
32 | MC-09KL32 | MC-09KR32 |
35 | MC-09KL35 | MC-09KR35 |
37 | MC-09KL37 | MC-09KR37 |
39 | MC-09KL39 | MC-09KR39 |
41 | MC-09KL41 | MC-09KR41 |
Advantages
Compared with traditional double-lumen tubes, the video channel
design increases the first-time intubation success rate by 40% and
reduces the average positioning time by 50%. Medical-grade PU
material increases the flexibility of the catheter by 30%, reducing
the risk of airway injury. The integrated design prevents
additional instruments from entering the airway, reducing the
chance of contamination. The low-pressure design of the airbag
reduces the incidence of mucosal compression injury to 0.5%. The
radiopaque marker reduces the X-ray positioning error to less than
1mm. The product has passed the biocompatibility test and the
cytotoxic reaction is level 0. In terms of cost-effectiveness, the
single-use design avoids the risk of cross-infection and reduces
the cost of cleaning and disinfection. A full range of
specifications can meet the needs of all age groups from children
to adults.
Serve
The manufacturer provides comprehensive technical support:
technical inquiries are responded to within 24 hours, and free
sample trials are available. Customized services include corporate
logo printing and custom specifications (length/diameter/curvature
adjustment).
Logistics support is guaranteed, with 48-hour delivery for urgent
orders, and temperature and humidity monitoring throughout
transportation. After-sales service includes clinical training
videos and online guidance from dedicated clinical engineers.
Product quality commitment: third-party test reports are provided,
and unconditional returns and exchanges are available for quality
issues.
Customer usage records are established, with product expiration
reminders three months in advance. Customized intubation carts are
provided for large hospitals, integrating related equipment to
improve operational efficiency.
FAQ
Q: What is the maximum usage time of the catheter?
A: It is recommended not to exceed 72 hours. Long-term use requires
monitoring of the cuff pressure.
Q: Is it compatible with all bronchoscopes?
A: It is compatible with electronic bronchoscopes and fiberscopes
with a diameter of ≤1.8mm.
Q: How to deal with difficult airway?
A: It is recommended to use the tube stylet to shape the tube
before intubation, and the video channel to assist in confirming
the position.
Q: How often should the cuff pressure be monitored?
A: It is recommended to monitor it every 4 hours and maintain a
pressure between 25-30 cmH₂O.
Q: Is it suitable for pediatric patients?
A: The 28FR specification is suitable for children weighing more
than 25 kg.
Q: What should I do if my blood oxygen level drops after tube
placement?
A: Immediately check the tube position and confirm whether the
non-ventilated lung is completely collapsed.
Q: How to confirm the correct position?
A: It is recommended to combine auscultation, fiberoptic
bronchoscopy and end-tidal CO₂ monitoring to make a comprehensive
judgment.