Additional Information; Application Instructions - Novatech TONN Mode D'emploi

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15.11 Storage
After sterilization, store the product dry and dust-free in the sterilization packaging.

15.12 Additional Information

Does not apply.
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Application Instructions

WARNING
• The product is not sterile. Process the product before first and any further application.
This is the only way to ensure the product is germ-free and functional.
• Only use intact products from intact sterile packaging or sterilization containers. Only use products that have not expired in
terms of their sterilization shelf life.
This is the only way to ensure the product is germ-free and functional.
• Check the product and all products used in combination before and after each use for integrity, completeness and proper
functioning (e.g. unintended coarse or sharp-edged surfaces, loose or incorrectly fitting parts and other obvious damage). Only
use impeccable products.
Otherwise there are risks for the health of your patient.
• Do not bend the instruments by applying excessive pressure. Do not bend back deformed instruments.
Otherwise, injury may be caused to the patient and user.
• Always correctly assemble the product and all products used in combination with it, including their components.
Otherwise there are risks for the health of your patient.
• Do not leave any parts in the patient.
Otherwise there are risks for the health of your patient.
• Only combine TONN NOVATECH components with the same color marking.
In case of incompatibility, perforation of the trachea/bronchi is possible.
• Use the product only with bronchoscopes / tracheoscopes of a suitable size.
In case of incompatibility, perforation of the bronchi / trachea is possible.
The manufacturer recommends using the product only together with the bronchoscopes/tracheoscopes recommended in the
specifications at the end of this document.
Use together with bronchoscopes / tracheoscopes other than the ones recommended here is the responsibility of the user.
Ensure the presence of hygienic / sterile conditions needed for the intervention.
Before using the product, perform a function test.
The intervention is performed under general anesthesia and fluoroscopic control (only for radiopaque stents).
16.1 Required Equipment and Materials
• Sterile, silicone-compatible, medical grade lubricant
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