-
PerFix™ Light Plug, Medium, 3.3 cm x 3.9 cm (1.3" x 1.6"), 6/case
-
PerFix™ Light Plug, Large, 4.1 cm x 4.8 cm (1.6" x 1.9"), 1/case
-
PerFix™ Light Plug, Large, 4.1 cm x 4.8 cm (1.6" x 1.9"), 6/case
-
PerFix™ Light Plug, Small, 2.5 cm x 3.4 cm (1.0" x 1.4"), 1/case
-
PerFix™ Light Plug, Extra Large, 3.8 cm x 5.0 cm (1.5" x 2.0"), 1/case
-
PerFix™ Light Plug, Medium, 3.3 cm x 3.9 cm (1.3" x 1.6"), 1/case
-
PerFix™ Light Plug, Small, 2.5 cm x 3.4 cm (1.0" x 1.4"), 6/case
-
PerFix™ Light Plug, Extra Large, 3.8 cm x 5.0 cm (1.5" x 2.0"), 6/case
Support
Sales
1.844.8.BD.LIFE (1.844.823.5433)
Thank you for contacting our sales team!
A sales representive will get in touch with you shortly.
Ordering
1.800.556.6756
BDISurgery@bd.com
Onsite Visiting
100 Crossings BoulevardWarwick, Rhode Island 02886United States
Customer Service
1.844.8.BD.LIFE (1.844.823.5433)
Monday to Friday 8:15 AM to 6:00 PM EST
1.800.531.4124
Custserv.davol@bd.com
Shipping a Product Back
100 Crossings Boulevard, Warwick, Rhode Island 02886, United States
PerFix™ Light Plug
Lighter-weight version of the proven PerFix™ Plug, for use when a reduced amount of material is indicated.
- Overview
- Products & Accessories
- EIFU & Resources
Live life tension-free
A lighter-weight version of our proven 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, customizing to patient.
- Tension-free repair achieved with Classic or Modified Techniques.
Trusted
- Same design as clinically-proven PerFix™ Plug, which has been used in over 5 million implants worldwide.1
- Proven design
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, such as groin 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.
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
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, such as groin 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.
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
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
Training
BD offers training resources to help improve your clinical practices as part of our goal of advancing the world of health.
Learn more
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 that excel in advancing the world of health™.
Learn more
Case Studies
BD promotes clinical excellence by providing various resources on best practices, clinical innovations and industry trends in healthcare.
Learn more
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, such as groin 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.
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