Stening® Tracheal Paediatric Stent

Code ST

Description

Small diameters, short length, thin wall, very flexible and transparent. With spurs arranged in a linear and opposite way.

image/svg+xml(units mm) D L W
References Dimensions (mm)
Translucent Radiopaque Diameter (D)Length (L)Wall thickness (W)
ST05-50 STX05-50 5500.5
ST06-50 STX06-50 6500.6
ST08-50 STX08-50 8500.8

For custom made devices you can contact us

Due to the characteristics of the production process,
the sizes of the devices may vary by +/- 2%

  • Tracheal or bronchial compression.
  • Airway obstruction of diverse aetiologies.

The procedure will be carried out under general anaesthesia.

Orotracheal intubation will be done with a rigid bronchoscope. The required length and the stent diameter should be properly determined.

The prosthesis can be folded and inserted into a previously lubricated prosthesis ejector, then expelled into the airway and close to the area that will be treated or apply it directly with the bronchoscope, sliding the stent its inside. The removal of the stent also requires access to the trachea with a rigid bronchoscope.

It is doubly simple because of the tiny dimensions of the device and, secondarily, the growth of the paediatric patient makes the stent able to free itself spontaneously.

An alligator forceps or similar will complete the removal manoeuvre.

Other implant and removal methods are possible depending on the surgeons experience and preferences.

Perform a periodic check-up following your doctor’s advice.

The product should not be reused because this can cause cross contamination.

Polymeric tracheal/bronchial stent, non-bioabsorbable, sterile
A sterile non-bioabsorbable tubular device intended to be implanted into the trachea and/or a bronchus/bronchiole to maintain luminal patency, typically used in cases of obstructions/stenoses, fistulae, tumours, scarring, surgical resection and anastomosis, or pulmonary transplantation. It is made entirely of a synthetic polymer(s) [e.g., silicone] and may have various designs (e.g., semi-soft continuous tube, covered or non-covered mesh structure, straight or branched configuration) intended to conform to the endotracheal/endobronchial surface. It may be expandable in situ (e.g., self-expands) and disposable devices intended to assist implantation may be included.

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