Same proven technique with improved mesh.
Bard© 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.
- Overview
- Specifications
- eIFUs and Resources
- FAQ
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FEATURE AND BENEFIT CARDS NOT AVAILABLE
FEATURE AND BENEFIT CARDS NOT AVAILABLE
GTIN - Case
00801741074424
1
Quantity
1/cs.
Dimensions
Medium with pocket 3.4" x 5.6" (8.6cm x 14.2cm)
GTIN
| GTIN - Case | 00801741074424 | 1 |
Packaging
| Quantity | 1/cs. |
Product Basic Specification
| Dimensions | Medium with pocket 3.4" x 5.6" (8.6cm x 14.2cm) |
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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
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 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 Onflex™ Mesh, except at the opening in the interrupted SorbaFlex™ PDO monofilament, to accommodate the spermatic cord and outside of the blue limit line in the lateral portion of the mesh, as this could affect its effectiveness. Care should be taken not to cut or nick the SorbaFlex™ PDO monofilament.
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.
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