Hiflux Nasal Splint - Medical Grade Silicone - Promni

Description:

The Hiflux Intranasal Splint is used in nasal septum correction surgeries. Designed to support the nasal septum cartilage in order to prevent the formation of edema and hematomas after surgery, restoring good ventilation to the nasal cavity after the surgical procedure. It can be easily removed according to medical procedure.

Benefits:

• Nasal breathing is permitted in the immediate postoperative period, provided airflow is not obstructed.
• Prevention of intranasal adhesions, which occur when scar tissue obstructs the nasal cavity.
• In the case of post-surgical bleeding, the product will ensure that the patient's airflow is not obstructed.
• Product that is easy to clean.
• It does not cause irritation or allergic reaction.
• Made from 100% medical-grade silicone.
• Made in Brazil.
• Sterilized with ethylene oxide.
  
  

Packaging:

The Hiflux Nasal Splint is presented in a single size in primary packaging in a Tyvek/LDPE-PET envelope containing two units (1 pair). The outer secondary packaging is in a cardboard box.

Mark

Promni

Manufacturer's Descriptive Brochure (Package Insert)

Click here to download the manufacturer's detailed leaflet and description containing measurements, instructions, recommendations, indications, and contraindications.

Contraindications:

Allergic reactions to silicone components.

WARNINGS:

Only the surgeon responsible for the procedure should choose, at their discretion, the technique that, in their experience, best suits the surgical procedure.

After using the product or before its expiration date, dispose of it immediately in accordance with current legal regulations.

Single-use product. Do not reprocess.

COMPOSITION: Silicone Elastomer

(Polydimethylsiloxane) medical grade, fully biocompatible, according to international standards.

Recommendations for the surgeon:

• Apply antibiotic ointment to the entire surface of the splint.

• Using your index finger and thumb or tweezers, flex the splint lengthwise and insert it into the nasal cavity.

• Suture the splint to the nasal cavity using the fixation holes located at the ends of the product.

• Maximum usage period recommended by the manufacturer: 10 days

ANVISA Registration No. 80112860010