Canada

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Ventralight™ Synthetic mesh Ventralight™ ST Mesh

Ventralight™ ST Mesh, Oval, 6" x 10" (15.2 cm x 25.4 cm)

Overview

Medium weight monofilament polypropylene mesh on the anterior side with an absorbable hydrogel barrier based on Sepra® Technology on the posterior side for laparoscopic ventral hernia repair.

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Features and Benefits
FEATURE AND BENEFIT CARDS NOT AVAILABLE
FEATURE AND BENEFIT CARDS NOT AVAILABLE
Promotional Story
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Specification

GTIN - Case

00801741183867

1

Quantity

1/cs

Dimensions

6” x 10” (15.2cm x 25.4cm) Oval

GTIN

GTIN - Case 00801741183867 1

Packaging

Quantity 1/cs

Product Basic Specification

Dimensions 6” x 10” (15.2cm x 25.4cm) Oval
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
productcomplaints@bd.com
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
References

* Preclinical data on file at BD. Results may not correlate to performance in humans.

** Based on a preclinical study of a composite polypropylene/ePTFE hernia repair mesh.

INDICATIONS

Ventralight™ ST Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.

CONTRAINDICATIONS

  1. Do not use the Ventralight™ ST in infants or children whereby future growth will be compromised by use of such material.
  2. Do not use Ventralight™ ST Mesh for the reconstruction of cardiovascular defects.
  3. Literature reports there may be a possibility for adhesion formation when the polypropylene is placed in direct contact with the bowel or viscera.

WARNINGS

  1. Ensure proper orientation; the coated side of the prosthesis should be oriented against the bowel or sensitive organs. Do not place the polypropylene side against the bowel. There may be a possibility for adhesion formation when the polypropylene side is placed in direct contact with the bowel or viscera.
  2. If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the prosthesis. An unresolved infection may require removal of the prosthesis. Possible complications include seroma, adhesions, hematomas, inflammation, extrusion, fistula formation and recurrence of the hernia or soft tissue defect.

  3. >strong>ADVERSE REACTIONS

    Possible complications include seroma, adhesions, hematomas, inflammation, extrusion, fistula formation, infection, allergic reaction, and recurrence of the hernia or soft tissue defect.

    Please consult package insert for more detailed safety information and instructions for use.

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