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Video-enabled Double-lumen Endotracheal Intubation ISO13485 Certified

Video-enabled Double-lumen Endotracheal Intubation ISO13485 Certified

Nombre De La Marca:	MCREAT
Número De Modelo:	En el caso de los vehículos de la categoría M1, el vehículo de la categoría M2 será el siguiente:
Cuota De Producción:	500
Precio:	USD 11.5-15.5/PC
Condiciones De Pago:	Moneygram, Western Union, T/T
Capacidad De Suministro:	200000pcs/mes

Información detallada

Descripción del producto

Información detallada

Lugar de origen:

PORCELANA

Certificación:

CE/FDA/ISO

Consejo:

azul suave

Clasificación:

Clase II

Solicitud:

Endotraqueal

Método de esterilización:

Óxido de etileno

ODM:

Sí

OEM:

Sí

Impresión del logotipo:

con o sin impresión de logotipo

Material:

PVC de grado médico

Detalles de empaquetado:

1 pieza por bolsa esterilizada, 10 piezas por caja interior, embalaje exterior: 100 piezas

Capacidad de la fuente:

200000pcs/mes

Descripción del producto

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
Size(FR)	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.

Las etiquetas:

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Sistema de succión cerrado

tubo endotraqueal

Vía aérea laríngea de la máscara

El cepillo de dientes de succión

Sistema de línea de succión

Tener el tubo endotraqueal

Bolsa de inyección de presión

Tubo bloqueador endobronquial

Tubo endobronquial de doble luz

Estillo de intubación endotraqueal

cánula nasal del alto flujo

Tubo nasofaríngeo de la vía aérea

Tubo de alimentación

catéter cerrado de la succión

Sistema de succión cerrado

tubo endotraqueal

Vía aérea laríngea de la máscara

El cepillo de dientes de succión

Sistema de línea de succión

Tener el tubo endotraqueal

Bolsa de inyección de presión

Tubo bloqueador endobronquial

Tubo endobronquial de doble luz

Estillo de intubación endotraqueal

cánula nasal del alto flujo

Tubo nasofaríngeo de la vía aérea

Tubo de alimentación

catéter cerrado de la succión

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Video-enabled Double-lumen Endotracheal Intubation ISO13485 Certified

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