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111781045: Teleflex Rusch AGT Nasal Preformed Cuffed Endotracheal Tube (ETT), High Volume, Low Pressure, Murphy Eye 4.5mm
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| Price: | $4.00 EACH |
|---|---|
| Quantity: | |
| In Stock: | 19 eaches |
| Expiration: | 10-2028 (or later) |
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Additional Details
Teleflex Rusch AGT Nasal Preformed Cuffed Endotracheal Tube (ETT)
Made of PVC with high volume, low pressure cuff
These anatomically shaped tubes have a high-volume, low-pressure cuff in both cylindrical and tapered styles and are designed to provide an optimal seal at low pressures.
- Single-use
- Sterile
- Not made with natural rubber latex.
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use
- Disposable
Additional Details
- Company Name: Teleflex Incorporated
- FDA Product Code: BTR
- FDA Product Code Name: Tube, tracheal (w/wo connector)
- GMDN Term Code: 46967
- GMDN Term Name: Basic endotracheal tube, single-use
- GMDN Term Definition: A hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated; it does not include an antimicrobial agent(s). The device may: 1) be packaged with a connector that will attach to a breathing circuit or manual resuscitator; 2) have a distal inflatable cuff to seal against the tracheal wall; 3) be radiopaque; and 4) have a built-in pilot balloon for cuff pressure monitoring. It is available in various diameters and lengths for adult and paediatric patients. This is a single-use device.
AccessGUDID Info
- FDA Product Code: BTR
- FDA Product Code Name: Tube, tracheal (w/wo connector)
- GMDN Term Code: 46967
- GMDN Term Name: Basic endotracheal tube, single-use
- GMDN Term Description: A hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated; it does not include an antimicrobial agent(s). The device may: 1) be packaged with a connector that will attach to a breathing circuit or manual resuscitator; 2) have a distal inflatable cuff to seal against the tracheal wall; 3) be radiopaque; and 4) have a built-in pilot balloon for cuff pressure monitoring. It is available in various diameters and lengths for adult and paediatric patients. This is a single-use device.
Manufacturer
Teleflex is a global leader in medical technology, providing innovative solutions to improve patient outcomes and enhance procedural efficiency. Specializing in critical care, interventional, and surgical devices, Teleflex offers a diverse portfolio designed to address complex healthcare needs.
Key products include Arrow® vascular access catheters, UroLift® System for minimally invasive treatment of benign prostatic hyperplasia (BPH), and Weck® ligation systems for surgical applications. Committed to advancing healthcare, Teleflex empowers clinicians with reliable, high-quality tools that drive better care across a wide range of specialties.
Teleflex Medical brands include: Arrow, Dekantel, Gibeck, Hudson RCI, KMedic, Pilling, Pleur-Evac, Rusch, Taut, Vasonova VPS and Weck
