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
PerFix™ Light Plug

Lighter-weight version of the proven PerFix™ Plug, for use when a reduced amount of material is indicated.

Contact Us navigation arrow
Carousel Image
Loading
tabs dropdown arrow
Overview

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.

Features and Benefits
Lighter weight
Lighter weight
  • Lighter-weight monofilament polypropylene mesh.
  • Reduced amount of implanted material.
  • Approximately 50% lighter than PerFix™ Plug.
Flexible
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
Reference

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

Products & Accessories
  • product-image

    PerFix™ Light Plug, Medium, 3.3 cm x 3.9 cm (1.3" x 1.6"), 6/case

  • product-image

    PerFix™ Light Plug, Large, 4.1 cm x 4.8 cm (1.6" x 1.9"), 1/case

  • product-image

    PerFix™ Light Plug, Large, 4.1 cm x 4.8 cm (1.6" x 1.9"), 6/case

  • product-image

    PerFix™ Light Plug, Small, 2.5 cm x 3.4 cm (1.0" x 1.4"), 1/case

  • product-image

    PerFix™ Light Plug, Extra Large, 3.8 cm x 5.0 cm (1.5" x 2.0"), 1/case

  • product-image

    PerFix™ Light Plug, Medium, 3.3 cm x 3.9 cm (1.3" x 1.6"), 1/case

  • product-image

    PerFix™ Light Plug, Small, 2.5 cm x 3.4 cm (1.0" x 1.4"), 6/case

  • product-image

    PerFix™ Light Plug, Extra Large, 3.8 cm x 5.0 cm (1.5" x 2.0"), 6/case

Related Products

References

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

Resources
References

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

Chat with us
Our live chat is available between the hours of 8.30am - 5.00pm EST, Monday - Friday
×