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Body surface conduit fixing device – Type I

The Body Surface Conduit Fixing Device - Type I is a sterile, single-use mechanical fixation system specifically designed for securing endotracheal tubes and other oral conduits in patients requiring airway management . Constructed from a rigid shell housing containing an integrated bite block, a sponge pad for patient comfort, a rotating nut and slider for tube clamping, and adjustable cheek fixation straps, the Type I device provides comprehensive oral tube securement that replaces traditional adhesive tape fixation methods.
For the anesthesiologist, respiratory therapist, and intensive care unit (ICU) nurse, Type I provides a mechanical alternative to tape fixation for intubated patients. The integrated bite block prevents the patient from occluding the endotracheal tube by biting down , while the rotating nut and slider mechanism allows precise tension adjustment of the clamping force around the tube . The cheek straps wrap around the patient's head or face to secure the entire assembly, eliminating the need for adhesive tape on the face—a significant advantage for patients requiring prolonged intubation, those with facial burns or skin trauma, or those with known adhesive allergies .
For the patient, Type I offers a more secure and comfortable alternative to traditional tape fixation. The bite block prevents the distressing event of tube occlusion from biting, which can trigger ventilator alarms and require emergency intervention. The sponge cushion reduces pressure on the face and lips, decreasing the risk of pressure ulcers and skin breakdown during extended intubation periods. The adjustable straps accommodate changes in facial edema and can be loosened or tightened without complete device removal, reducing disturbance to the patient. Available in multiple configurations including specifications as a Class II medical device , Type I is the catheter fixation device of choice for endotracheal tube management in intensive care, operating rooms, emergency departments, and during patient transport, particularly for patients where facial skin preservation and secure tube fixation are both clinical priorities.