-
PerFix™ Plug, Small, 1.0" x 1.35" (2.5cm x 3.4cm), 2/case
-
PerFix™ Plug, Extra Large, 1.6" x 2.0" (4.1cm x 5.0cm), 6/case
-
PerFix™ Plug, Large, 1.6" x 1.90" (4.1cm x 4.8cm), 6/case
-
PerFix™ Plug, Small, 1.0" x 1.35" (2.5cm x 3.4cm), 6/case
-
PerFix™ Plug, Large, 1.6" x 1.90" (4.1cm x 4.8cm), 2/case
-
PerFix™ Plug, Extra Large, 1.6" x 2.0" (4.1cm x 5.0cm), 2/case
-
PerFix™ Plug, Medium, 1.3" x 1.55" (3.3cm x 3.9cm), 6/case
-
PerFix™ Plug, Medium, 1.3" x 1.55" (3.3cm x 3.9cm), 2/case
true
PerFix™ Plug
Plug and patch designed for use in a tension-free open inguinal hernia repair technique.
- Overview
- Products & Accessories
- EIFU & Resources
- FAQ
A quick and simple preperitoneal underlay Modified Technique for the repair of groin hernias
The PerFix™ Plug is ideal for use in a tension-free preperitoneal repair technique. With over five million implants worldwide, the Bard™ PerFix™ Plug is designed with pleated edges that conform readily to defects of various sizes and shapes. The monofilament polypropylene design ensures healthy tissue ingrowth.
true
Efficient
Entire operation can take 25 minutes or less2 Minimal dissection is required 4-5cm incision1 Local or epidural anesthesia can be used Accommodates all types of groin hernias
Effective
Utilized in a tension-free repair technique Recurrence rates reported at 0.15%1 Less than 0.5% chronic pain rate1
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.
2. Rutkow, I.M. : The Perfix plug repair for groin hernias. Surg Clinics of N. America, 2003; 83; 5: 1079-1098; 78; 6: 1007-1023
INDICATIONS
This product is indicated for the repair of groin hernia defects.
CONTRAINDICATIONS
Literature reports that there may be a possibility for adhesion formation when Bard® mesh is placed in direct contact with the bowel or viscera.
Do not use the PerFix™ 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™ Plug
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematoma, 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
BD-14804
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.
2. Rutkow, I.M. : The Perfix plug repair for groin hernias. Surg Clinics of N. America, 2003; 83; 5: 1079-1098; 78; 6: 1007-1023
INDICATIONS
This product is indicated for the repair of groin hernia defects.
CONTRAINDICATIONS
Literature reports that there may be a possibility for adhesion formation when Bard® mesh is placed in direct contact with the bowel or viscera.
Do not use the PerFix™ 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™ Plug
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematoma, 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
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.
2. Rutkow, I.M. : The Perfix plug repair for groin hernias. Surg Clinics of N. America, 2003; 83; 5: 1079-1098; 78; 6: 1007-1023
INDICATIONS
This product is indicated for the repair of groin hernia defects.
CONTRAINDICATIONS
Literature reports that there may be a possibility for adhesion formation when Bard® mesh is placed in direct contact with the bowel or viscera.
Do not use the PerFix™ 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™ Plug
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematoma, 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
false
true
