Loading
{"AlternateComparison":false,"RelatedProducts":true,"Specification":true,"FeatureBenefit":false}
OnFlex™ Synthetic mesh Modified OnFlex™ Mesh

Modified OnFlex™ Mesh with Pocket, Strap, and Onlay, Large, 10.2 cm x 15.7 cm

Icon to close the modal
Support
Sales
Phone Icon
1.844.8.BD.LIFE (1.844.823.5433)
Modal Close Icon
Sales Form
Please fill out the form and a sales representative will get in touch with you.

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 Boulevard Warwick, Rhode Island 02886 United 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
tabs dropdown arrow
Overview
Same proven technique with improved mesh

Bard© Modified OnFlex ™ Mesh was specifically designed to fit the inguinal anatomy during preperitoneal placement. It offers extended medial and inferior coverage for direct and femoral hernia spaces.

true
Features and Benefits
Promotional Story
false
References

1. Brown C, Finch J. Which mesh for hernia repair? Annals of The Royal College of Surgeons of England 2010;92(4):272-278.

* Observed in preclinical model, which may not correlate to performance in humans.

Indications

The Modified Onflex™ Mesh is indicated for use in the reinforcement of soft tissue where weakness exists, such as in the repair of inguinal hernias.

Contraindications

Use of this device is contraindicated for infants, children, or pregnant women, whereby future growth will be compromised by use of such mesh material. Literature reports that there is a possibility for adhesion formation when polypropylene is placed in direct contact with the bowel or viscera.

Warnings

The use of any synthetic mesh or patch in a contaminated or infected wound can lead to fistula formation and/or extrusion of the mesh and is not recommended. If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the mesh. Unresolved infection may require removal of the mesh.

Do not cut or reshape the Modified Onflex™ Mesh, except for the positioning strap, as this could affect its effectiveness. Care should be taken not to cut or nick the SorbaFlex™ PDO monofilament

Excess positioning strap material above the fixation point must be cut off at the level of the fascia and discarded to eliminate excess material from remaining in the body.

Precautions

Care should be taken not to cut or nick the SorbaFlex™ PDO monofilament.

Adverse Reactions

Possible complications may include, but are not limited to, seroma, adhesion, hematoma, pain, infection, inflammation, extrusion, erosion, migration, fistula formation and recurrence of the hernia or soft tissue defect. If the SorbaFlex™ PDO monofilament is cut or damaged, additional complications may include, but are not limited to, bowel or skin perforation and infection.

true
Specification

GTIN - Case

00801741095405

1


Quantity

1/cs.


Dimensions

Large with pocket, strap & onlay 4.0" x 6.2" (10.2cm x 15.7cm)

GTIN

GTIN - Case 00801741095405 1

Packaging

Quantity 1/cs.

Product Basic Specification

Dimensions Large with pocket, strap & onlay 4.0" x 6.2" (10.2cm x 15.7cm)
References
false
Resources
References
false
Frequently Asked Questions
false
References
false
Related Products
  • product-image

    OnFlex™ Mesh, Medium, 8.6 cm x 14.2 cm

  • product-image

    OnFlex™ Mesh, Large, 10.2 cm x 15.7 cm

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
Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
navigation arrow
References
false
Chat with us
Our live chat is available between the hours of 8.30am - 5.00pm EST, Monday - Friday
×