{"AlternateComparison":false,"RelatedProducts":true,"Specification":true,"FeatureBenefit":false}
Composix™ Synthetic mesh Composix™ E X Mesh

Composix™ E/X Mesh, Elliptical, 7 in x 9 in (18 cm x 23 cm)

Icon to close the modal
Support
Sales
Phone Icon
1.844.8.BD.LIFE (1.844.823.5433)
Modal Close Icon

Capability:

Product Line:

Icon to close thank you modal
Thank you for contacting our sales team!
A sales representive will get in touch with you shortly.
Ordering
Phone Icon
1.800.556.6756
BDISurgery@bd.com
Onsite Visiting
Location Icon
100 Crossings BoulevardWarwick, Rhode Island 02886United States
Customer Service
Phone Icon
1.844.8.BD.LIFE (1.844.823.5433)
Monday to Friday 8:15 AM to 6:00 PM EST
Fax Icon
1.800.531.4124
Custserv.davol@bd.com
Shipping a Product Back
Location Icon
100 Crossings Boulevard, Warwick, Rhode Island 02886, United States
Overview

Polypropylene and Permanent ePTFE Barrier Designed for Ventral Hernia Repair

The Bard™ Composix™ E/X Mesh, combines two clinically proven biomaterials, Bard™ polypropylene mesh and ePTFE, into one product. The polypropylene side of the Bard™ Composix™ E/X Mesh promotes tissue ingrowth into the abdominal wall over time and eliminates the need for transfixation sutures. The visceral side of the Bard™ Composix™ E/X Mesh features a permanent submicronic ePTFE barrier, which minimizes attachments to the prosthesis. This ePTFE barrier is permanent, offering long-term protection.

true
Features and Benefits
Promotional Story
false
References

INDICATIONS

Bard™ Composix™ E/X Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias and chest wall defects.

CONTRAINDICATIONS

Literature reports there may be a possibility for adhesion formation when the polypropylene is placed in direct contact with the bowel or viscera.

Do not use the Bard™ Composix™ E/X Mesh, in infants or children whereby future growth will be compromised by use of such material.

Do not use Bard™ Composix™ E/X Mesh, for the reconstruction of cardiovascular defects.

WARNINGS

Ensure proper orientation; the solid white surface (ePTFE) must be oriented against the bowel or sensitive organs. Do not place the polypropylene mesh surface against the bowel or sensitive organs. There may be a possibility for adhesion formation when polypropylene mesh is placed in direct contact with the bowel or viscera.

If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the mesh. An unresolved infection may require removal of the device.

PRECAUTIONS

DAVOL™ fixation devices or nonabsorbable monofilament sutures are recommended to properly secure the prosthesis. If other fixation devices are used, they must be indicated for use in hernia repair. Care should be taken to ensure that the prosthesis is adequately fixated to the abdominal wall. If necessary, additional fasteners and/or sutures should be used.

ADVERSE REACTIONS

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

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

true
Specification

GTIN - Case

00801741031205

1


Quantity

1/cs.


Dimensions

7" x 9" (18 cm x 23 cm) Elliptical

GTIN

GTIN - Case 00801741031205 1

Packaging

Quantity 1/cs.

Product Basic Specification

Dimensions 7" x 9" (18 cm x 23 cm) Elliptical
References
false
Electronic Instructions for Use (eIFUs)
Resources
References
false
Frequently Asked Questions
false
References
false
Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
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
Product Recalls
Literature Icon
Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
References
false
false