Aftercare - Novatech TONN Mode D'emploi

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17 Instructing the Patient
Does not apply.
18

Aftercare

Does not apply.
19 Disposal
Disposal must be in accordance with national disposal regulations and pursuant to the corresponding risk class.
20 Warranty
The reliability of the product's material and design at the time of shipment is guaranteed. The manufacturer does not know either
the diagnosis of the patient or the nature of the application and has no influence on the conditions under which the product is used.
The storage conditions after delivery of the product are also beyond the manufacturer's area of responsibility.
Due to biological and individual differences, no product is 100% effective under all circumstances.
Therefore, the manufacturer cannot guarantee a positive effect or the absence of negative effects for product application. The
medical staff must use the product on the basis of their medical training and experience, and they are responsible for correct
application.
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4. Pull out the introducer tube from the folding device. The distal end of
the stent closes flush with the distal end of the introducer tube.
5. Introduce the pusher until a resistance is felt at the proximal end of the
introducer tube. The scale on the pusher shows the length of the stent.
6. Introduce the introducer tube into the bronchoscope. Push the pusher to
push the stent out of the introducer tube. The stent will fold.
For TD / TF ≥ 18 mm, Y, OKI type stents: Use the NOVATECH logo on the
introducer tube as a guide.