Description
Therapeutic administration of oxygen nasally.
Single-use product (for a single patient), to be used continuously for a period not exceeding 30 days.
Oxygen delivery systems must comply with current regulations.
Products must be used by qualified healthcare personnel.
Latex free.

Instructions for use
Gently insert the appropriate terminals of the nasal dispenser into each nostril and proceed for each model as described below.
Keep the nasal dispenser terminals in position and pass both the right and left tubes around the respective auricles, then guide them down along the mandibular arches to the submental region. Adjust the tension using the plastic positioning ring.
Insert the connector at the end of the appropriate connecting tube onto the oxygen delivery device's outlet. After connecting the device, deliver oxygen, adjusting the flow as needed.

Warnings
Reusing the product, contrary to these instructions, may lead to:
- alterations of materials;
- non-cleaning of the device and possible presence of biological residues that can cause cross-infections;
- loss of the product's initial functional characteristics.
Before connecting to the oxygen delivery device, check its operation. Accidental crushing or kinking of the connecting tube will prevent the regular passage of oxygen and may cause the connector to detach from the delivery device. Therefore, careful monitoring by users is recommended. This warning applies even though the models are equipped with an anti-kink star lumen tube, which reduces, but does not eliminate, the risk of flow interruption.
This product contains phthalates (DEHP). While no risks to human health have been confirmed, the long-term use of devices on pregnant/breastfeeding women or children should be evaluated by the treating physician.
The use of nasal cannulas may be associated with epistaxis in individuals predisposed to bleeding and/or undergoing anticoagulant therapy.
Concentrated oxygen can cause combustible materials to ignite. To avoid risks of fire or explosion, keep away from possible ignition sources, and refer to the usage precautions of the equipment used for oxygen delivery.
The product must be stored in its original packaging in premises characterized by environmental conditions, temperature, and relative humidity, as specified on the label on the packaging.
Stacking weights on the packaging could damage the product.
Complies with current European Medical Device regulations. If a serious incident occurs during or after the use of the device, report it to the Manufacturer and national authorities.
For any malfunction or defect of the device, inform the Manufacturer's Quality Department.
Waste from healthcare facilities must be disposed of according to current regulations.

Code 12360