true
{"AlternateComparison":false,"RelatedProducts":false,"Specification":true,"FeatureBenefit":false}
No image
Ventralight™ Synthetic mesh Ventralight™ ST Mesh

Ventralight™ ST Mesh, Rectangle, 12" x 14" (30.5 cm x 35.6 cm)

Icon to close the modal
Support
Becton Dickinson Australia & New Zealand
Phone Icon
AU: 1800 656 100
NZ: 0800 572 468
Submit a form online
Go next / move forward Icon
Modal Close Icon
Icon to close thank you modal
Thank you for contacting our sales team!
A sales representive will get in touch with you shortly.
For more information, please visit our Contact Us page
Contact Us
Go next / move forward Icon
Overview

Uncoated 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.

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

GTIN - Case

00801741031601

1

GTIN

GTIN - Case 00801741031601 1
Electronic Instructions for Use (eIFUs)
Resources
white-papers-boosted-blue.svg
Literature

BD’s collection of literature on industry and on our offerings give you information you can use to continue striving for excellence.

Learn more
events-boosted-blue.svg
Events

BD supports the healthcare industry with market-leading products and services that aim to improve care while lowering costs. We host and take part in events which excel in advancing the world of health™.

Learn more
Frequently Asked Questions
false
Related Products
RELATED PRODUCTS NOT AVAILABLE
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 in the repair of ventral, incisional and umbilical 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.
  4. This mesh is not for the use of repair of pelvic organ prolapse via transvaginal approach. This mesh is not for the use of treatment of stress urinary incontinence.

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. This mesh is not for the use of repair of pelvic organ prolapse via transvaginal approach.
  4. This mesh is not for the use of treatment of stress urinary incontinence.

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.

true
true