Optomesh^® STOMA

Optomesh^® STOMA

Surgical mesh for surgical treatment of parastomal hernia

CHARACTERISTIC

Optomesh^® STOMA non-resorbable surgical mesh knitted from transparent and blue monofilament polypropylene yarn. They are designed to treat parastomal hernias.

The assortment list contains one mesh size (195 mm x 195 mm), but the dimensions may be modified by the doctor during implantation in order to adjust the shapes to the individual patient's anatomy.

Optomesh^® STOMA device does not contain any substances of allogenic or animal origin. The applied blue orienting lines along the product facilitate visibility and positioning the product in the operating field.

INDICATIONS

Optomesh^® STOMA surgical meshes are intended for use in the surgical treatment of the causal or preventive occurrence of parastomal hernia. The most common indications for surgical treatment of hernias are: obstruction of intestinal passage, large hernia size, pain and discomfort while moving, chronic inflammatory changes around the stoma, entrapment episodes, and cosmetic considerations.

PRECAUTIONS

1. Optomesh^® STOMA mesh implant is intended for use by qualified and properly trained medical personnel.
2. In order to ensure strict surgical aseptic conditions during the procedure, it is advisable to apply special precautions (use of personal protection, sterilization of instruments, high personal hygiene) and extraordinary attention during the preparation of the site of direct intervention by the surgeon.
3. Optomesh^® STOMA surgical meshes should be used only in uninfected wounds and in conditions where strict surgical aseptic conditions are possible.
4. Do not implant Optomesh^® STOMA surgical meshes after the expiration date.
5. Optomesh^® STOMA polypropylene surgical meshes are offered for sale in a sterile state. The product cannot be re-sterilized.
6. The product is for single use only.
7. A product that is damaged, dirty or with defects in its structure cannot be used (increased tightness of the knitted fabric does not constitute a product defect).

STERILIZATION

Sterilization is done with Ethylene Oxide (EO) in a validated process.

The product remains sterile until the expiry date, only in its original packaging, under appropriate storage conditions.

Optomesh^® STOMA

Surgical mesh for surgical treatment of parastomal hernia

CHARACTERISTIC

Optomesh^® STOMA non-resorbable surgical mesh knitted from transparent and blue monofilament polypropylene yarn. They are designed to treat parastomal hernias.

The assortment list contains one mesh size (195 mm x 195 mm), but the dimensions may be modified by the doctor during implantation in order to adjust the shapes to the individual patient's anatomy.

Optomesh^® STOMA device does not contain any substances of allogenic or animal origin. The applied blue orienting lines along the product facilitate visibility and positioning the product in the operating field.

INDICATIONS

Optomesh^® STOMA surgical meshes are intended for use in the surgical treatment of the causal or preventive occurrence of parastomal hernia. The most common indications for surgical treatment of hernias are: obstruction of intestinal passage, large hernia size, pain and discomfort while moving, chronic inflammatory changes around the stoma, entrapment episodes, and cosmetic considerations.

PRECAUTIONS

1. Optomesh^® STOMA mesh implant is intended for use by qualified and properly trained medical personnel.
2. In order to ensure strict surgical aseptic conditions during the procedure, it is advisable to apply special precautions (use of personal protection, sterilization of instruments, high personal hygiene) and extraordinary attention during the preparation of the site of direct intervention by the surgeon.
3. Optomesh^® STOMA surgical meshes should be used only in uninfected wounds and in conditions where strict surgical aseptic conditions are possible.
4. Do not implant Optomesh^® STOMA surgical meshes after the expiration date.
5. Optomesh^® STOMA polypropylene surgical meshes are offered for sale in a sterile state. The product cannot be re-sterilized.
6. The product is for single use only.
7. A product that is damaged, dirty or with defects in its structure cannot be used (increased tightness of the knitted fabric does not constitute a product defect).

STERILIZATION

Sterilization is done with Ethylene Oxide (EO) in a validated process.

The product remains sterile until the expiry date, only in its original packaging, under appropriate storage conditions.