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PerFix™ Light Plug
Lighter-weight version of the proven PerFix™ Plug, for use when a reduced amount of material is indicated.
- Overview
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Live life tension-free
A lighter-weight version of our PerFix™ Plug for tension-free inguinal hernia repair. The PerFix™ Light Plug is ideal for use in a tension-free preperitoneal repair technique where a lighter-weight mesh and reduced amount of implanted material is indicated.
Lighter weight
- Lighter-weight monofilament polypropylene mesh.
- Reduced amount of implanted material.
- Approximately 50% lighter than PerFix™ Plug.
Flexible
- Dynamic design conforms to defect.
- Inner petals and onlay patch can be trimmed, customising to patient.
- Tension-free repair achieved with Classic or Modified Techniques.
1. Millikan KW, Doolas A. A Long-Term Evaluation of the Modified Mesh-Plug Hernioplasty in Over 2,000 Patients. Hernia. 2008 June; 12(3): 257-260.
INDICATIONS
The PerFix™ Light Plug is indicated for reinforcement of soft tissue, where weakness exists, in procedures involving soft tissue repair of inguinal hernia defects.
CONTRAINDICATIONS
Literature reports that there may be a possibility for adhesion formation when polypropylene mesh is placed in direct contact with the bowel or viscera. Do not use the PerFix™ Light Plug in infants or children, whereby future growth will be compromised by use of such mesh material.
WARNINGS
The use of any permanent mesh or patch in a contaminated or infected wound could lead to fistula formation and/or extrusion of the mesh.
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.
This device is not for the use of repair of pelvic organ prolapse. This device is not for the use of treatment of stress urinary incontinence
PRECAUTIONS
Monofilament sutures are recommended to properly secure the PerFix™Light Plug
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, infection, pain, mesh migration, 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
BD-116116
1. Millikan KW, Doolas A. A Long-Term Evaluation of the Modified Mesh-Plug Hernioplasty in Over 2,000 Patients. Hernia. 2008 June; 12(3): 257-260.
INDICATIONS
The PerFix™ Light Plug is indicated for reinforcement of soft tissue, where weakness exists, in procedures involving soft tissue repair of inguinal hernia defects.
CONTRAINDICATIONS
Literature reports that there may be a possibility for adhesion formation when polypropylene mesh is placed in direct contact with the bowel or viscera. Do not use the PerFix™ Light Plug in infants or children, whereby future growth will be compromised by use of such mesh material.
WARNINGS
The use of any permanent mesh or patch in a contaminated or infected wound could lead to fistula formation and/or extrusion of the mesh.
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.
This device is not for the use of repair of pelvic organ prolapse. This device is not for the use of treatment of stress urinary incontinence
PRECAUTIONS
Monofilament sutures are recommended to properly secure the PerFix™Light Plug
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, infection, pain, mesh migration, 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
BD-14805
true
Literature
BD's collection of literature on industry and on our offerings gives you information you can use to continue striving for excellence.
Learn more
true
1. Millikan KW, Doolas A. A Long-Term Evaluation of the Modified Mesh-Plug Hernioplasty in Over 2,000 Patients. Hernia. 2008 June; 12(3): 257-260.
INDICATIONS
The PerFix™ Light Plug is indicated for reinforcement of soft tissue, where weakness exists, in procedures involving soft tissue repair of inguinal hernia defects.
CONTRAINDICATIONS
Literature reports that there may be a possibility for adhesion formation when polypropylene mesh is placed in direct contact with the bowel or viscera. Do not use the PerFix™ Light Plug in infants or children, whereby future growth will be compromised by use of such mesh material.
WARNINGS
The use of any permanent mesh or patch in a contaminated or infected wound could lead to fistula formation and/or extrusion of the mesh.
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.
This device is not for the use of repair of pelvic organ prolapse. This device is not for the use of treatment of stress urinary incontinence
PRECAUTIONS
Monofilament sutures are recommended to properly secure the PerFix™Light Plug
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, infection, pain, mesh migration, 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
BD-14805
true
